Allele Registry

Canonical Allele Identifier: CA11076662

Gene:

Linked Data - Expert Curation

COSMIC:

COSN6671388 (not active)

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr2:g.102410643T>C

GRCh37 chr2:g.103027103T>C

Linked Data - Sequence & Population

gnomAD v2:

2:103027103 T / C

gnomAD v3:

2:102410643 T / C

gnomAD v4:

chr2-102410643-T-C

Joint Max Group AF 0.88635742 (AFR)

Genomes Max Group AF 0.88635742 (AFR)

Linked Data - NCBI & NCI

dbSNP:

6419573

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102410643T>C , CM000664.2:g.102410643T>C	GRCh38
NC_000002.11:g.103027103T>C , CM000664.1:g.103027103T>C	GRCh37
NC_000002.10:g.102393535T>C	NCBI36

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