Allele Registry

Canonical Allele Identifier: CA13891515

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr13:g.105545886T>A

GRCh37 chr13:g.106198235T>A

Linked Data - Sequence & Population

gnomAD v2:

13:106198235 T / A

gnomAD v3:

13:105545886 T / A

gnomAD v4:

chr13-105545886-T-A

Joint Max Group AF 0.47368026 (AMR)

Genomes Max Group AF 0.47368026 (AMR)

Linked Data - NCBI & NCI

dbSNP:

1421292

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.105545886T>A , CM000675.2:g.105545886T>A	GRCh38
NC_000013.10:g.106198235T>A , CM000675.1:g.106198235T>A	GRCh37
NC_000013.9:g.104996236T>A	NCBI36

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