Allele Registry

Canonical Allele Identifier: CA10939617

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr1:g.59249320T>C

GRCh37 chr1:g.59714992T>C

Linked Data - Sequence & Population

gnomAD v2:

1:59714992 T / C

gnomAD v3:

1:59249320 T / C

gnomAD v4:

chr1-59249320-T-C

Joint Max Group AF 0.835078 (NFE)

Genomes Max Group AF 0.835078 (NFE)

Linked Data - NCBI & NCI

dbSNP:

1470407

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.59249320T>C , CM000663.2:g.59249320T>C	GRCh38
NC_000001.10:g.59714992T>C , CM000663.1:g.59714992T>C	GRCh37
NC_000001.9:g.59487580T>C	NCBI36

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