Allele Registry

Canonical Allele Identifier: CA527362796

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr1:g.172929187A>T

GRCh37 chr1:g.172898327A>T

Linked Data - Sequence & Population

gnomAD v2:

1:172898327 A / T

gnomAD v3:

1:172929187 A / T

gnomAD v4:

chr1-172929187-A-T

Joint Max Group AF 0.00037949 (EAS)

Genomes Max Group AF 0.00037949 (EAS)

Linked Data - NCBI & NCI

dbSNP:

1333767147

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172929187A>T , CM000663.2:g.172929187A>T	GRCh38
NC_000001.10:g.172898327A>T , CM000663.1:g.172898327A>T	GRCh37
NC_000001.9:g.171164950A>T	NCBI36

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