Allele Registry

Canonical Allele Identifier: CA296148947

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr18:g.4777540T>C

GRCh37 chr18:g.4777539T>C

Linked Data - Sequence & Population

gnomAD v2:

18:4777539 T / C

gnomAD v3:

18:4777540 T / C

gnomAD v4:

chr18-4777540-T-C

Joint Max Group AF 0.92769036 (EAS)

Genomes Max Group AF 0.92769036 (EAS)

Linked Data - NCBI & NCI

dbSNP:

7504165

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.4777540T>C , CM000680.2:g.4777540T>C	GRCh38
NC_000018.9:g.4777539T>C , CM000680.1:g.4777539T>C	GRCh37
NC_000018.8:g.4767539T>C	NCBI36

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