Allele Registry

Canonical Allele Identifier: CA10692432

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr1:g.175150943A>C

GRCh37 chr1:g.175120079A>C

Linked Data - Sequence & Population

gnomAD v2:

1:175120079 A / C

gnomAD v3:

1:175150943 A / C

gnomAD v4:

chr1-175150943-A-C

Joint Max Group AF 0.45102612 (NFE)

Genomes Max Group AF 0.45102612 (NFE)

Linked Data - NCBI & NCI

dbSNP:

6701037

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.175150943A>C , CM000663.2:g.175150943A>C	GRCh38
NC_000001.10:g.175120079A>C , CM000663.1:g.175120079A>C	GRCh37
NC_000001.9:g.173386702A>C	NCBI36

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