Allele Registry

Canonical Allele Identifier: CA540914995

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr3:g.1470903C>G

GRCh37 chr3:g.1512587C>G

Linked Data - Sequence & Population

gnomAD v2:

3:1512587 C / G

gnomAD v3:

3:1470903 C / G

gnomAD v4:

chr3-1470903-C-G

Joint Max Group AF 0.00001922 (AFR)

Genomes Max Group AF 0.00001922 (AFR)

Linked Data - NCBI & NCI

dbSNP:

6763848

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.1470903C>G , CM000665.2:g.1470903C>G	GRCh38
NC_000003.11:g.1512587C>G , CM000665.1:g.1512587C>G	GRCh37
NC_000003.10:g.1487587C>G	NCBI36

Search 100 bp 5'

Search 100 bp 3'