Allele Registry

Canonical Allele Identifier: CA680374185

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr11:g.76600576G>C

GRCh37 chr11:g.76311620G>C

Linked Data - Sequence & Population

gnomAD v3:

11:76600576 G / C

gnomAD v4:

chr11-76600576-G-C

Linked Data - NCBI & NCI

dbSNP:

7124842

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.76600576G>C , CM000673.2:g.76600576G>C	GRCh38
NC_000011.9:g.76311620G>C , CM000673.1:g.76311620G>C	GRCh37
NC_000011.8:g.75989268G>C	NCBI36

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