Allele Registry

Canonical Allele Identifier: CA785872353

Gene:

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr4:g.116954105T>A

GRCh37 chr4:g.117875261T>A

Linked Data - Sequence & Population

gnomAD v3:

4:116954105 T / A

gnomAD v4:

chr4-116954105-T-A

Linked Data - NCBI & NCI

dbSNP:

1440306

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.116954105T>A , CM000666.2:g.116954105T>A	GRCh38
NC_000004.11:g.117875261T>A , CM000666.1:g.117875261T>A	GRCh37
NC_000004.10:g.118094709T>A	NCBI36

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