Genome

Gencode genome annotations:

• [ ] GRCh37/hg19

HUGO Gene Nomenclature Committee (HGNC)

1000 Genomes

• [ ] GRCh37/hg19

• [ ] GRCh38/hg38

• [ ] GRCh38/hg38

APPRIS gene isoforms For version hg19 (matched to Gencode version 19) For version hg38 (matched to Gencode version 31)

HapMap II recombination hotspots

LDlink LDproxy

**UCSC liftOver**

Giggle

Mendelian disease genes and variants

OMIM

Orphanet Rare diseases and cross referencing

[Linearisation of disorders](<http://www.orphadata.org/data/xml/en_product7.xml>)

[Rare diseases with their associated genes](<http://www.orphadata.org/data/xml/en_product6.xml>)

Genomics England

DECIPHER

ClinVar

Gene set enrichment