Allele Registry

Canonical Allele Identifier: CA11386815

Gene:

Linked Data

ClinVar RCV:

RCV001522189

RCV001709717

ClinVar Variation:

1170126

dbSNP:

5393

gnomAD v2:

3:170744920 T / G

gnomAD v3:

3:171027131 T / G

gnomAD v4:

chr3-171027131-T-G

Joint Max Group AF 0.46036717 (AFR)

Genomes Max Group AF 0.46036717 (AFR)

MyVariant.info:

GRCh38 chr3:g.171027131T>G

GRCh37 chr3:g.170744920T>G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.171027131T>G , CM000665.2:g.171027131T>G	GRCh38
NC_000003.11:g.170744920T>G , CM000665.1:g.170744920T>G	GRCh37
NC_000003.10:g.172227614T>G	NCBI36
NG_008108.1:g.4849A>C

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