Canonical Allele Identifier: CA906314285

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.3314490A>T , CM000665.2:g.3314490A>T	GRCh38
NC_000003.11:g.3356174A>T , CM000665.1:g.3356174A>T	GRCh37
NC_000003.10:g.3331174A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940546.1:n.337+22810T>A