Allele Registry

Canonical Allele Identifier: CA671462439

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr11:g.109076917G>C

GRCh37 chr11:g.108947644G>C

Linked Data - Sequence & Population

gnomAD v3:

11:109076917 G / C

gnomAD v4:

chr11-109076917-G-C

Linked Data - NCBI & NCI

dbSNP:

11212913

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.109076917G>C , CM000673.2:g.109076917G>C	GRCh38
NC_000011.9:g.108947644G>C , CM000673.1:g.108947644G>C	GRCh37
NC_000011.8:g.108452854G>C	NCBI36

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