Allele Registry

Canonical Allele Identifier: CA12313941

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr6:g.6331703T>C

GRCh37 chr6:g.6331936T>C

Linked Data - Sequence & Population

gnomAD v2:

6:6331936 T / C

gnomAD v3:

6:6331703 T / C

gnomAD v4:

chr6-6331703-T-C

Joint Max Group AF 0.61665103 (EAS)

Genomes Max Group AF 0.61665103 (EAS)

Linked Data - NCBI & NCI

dbSNP:

1318606

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6331703T>C , CM000668.2:g.6331703T>C	GRCh38
NC_000006.11:g.6331936T>C , CM000668.1:g.6331936T>C	GRCh37
NC_000006.10:g.6276935T>C	NCBI36

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