Allele Registry

Canonical Allele Identifier: CA11949950

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr5:g.159332892A>G

GRCh37 chr5:g.158759900A>G

Linked Data - Sequence & Population

gnomAD v2:

5:158759900 A / G

gnomAD v3:

5:159332892 A / G

gnomAD v4:

chr5-159332892-A-G

Joint Max Group AF 0.60428999 (AFR)

Genomes Max Group AF 0.60428999 (AFR)

Exomes Max Group AF 0.34560971 (NFE)

Linked Data - NCBI & NCI

dbSNP:

2546890

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159332892A>G , CM000667.2:g.159332892A>G	GRCh38
NC_000005.9:g.158759900A>G , CM000667.1:g.158759900A>G	GRCh37
NC_000005.8:g.158692478A>G	NCBI36
NG_009618.1:g.2582T>C , LRG_71:g.2582T>C

Transcript Alleles

HGVS	Amino-acid Change
NR_037889.1:n.634A>G

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