Allele Registry

Canonical Allele Identifier: CA11131891

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr2:g.171522147T>G

GRCh37 chr2:g.172378657T>G

Linked Data - Sequence & Population

gnomAD v2:

2:172378657 T / G

gnomAD v3:

2:171522147 T / G

gnomAD v4:

chr2-171522147-T-G

Joint Max Group AF 0.3544667 (AFR)

Genomes Max Group AF 0.35298535 (AFR)

Exomes Max Group AF 0.35290045 (AFR)

Linked Data - NCBI & NCI

dbSNP:

884409

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171522147T>G , CM000664.2:g.171522147T>G	GRCh38
NC_000002.11:g.172378657T>G , CM000664.1:g.172378657T>G	GRCh37
NC_000002.10:g.172086903T>G	NCBI36

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