Canonical Allele Identifier: CA72289808

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30605668A>T , CM000665.2:g.30605668A>T	GRCh38
NC_000003.11:g.30647160A>T , CM000665.1:g.30647160A>T	GRCh37
NC_000003.10:g.30622164A>T	NCBI36
NG_007490.1:g.4167A>T , LRG_779:g.4167A>T

Transcript Alleles

HGVS	Amino-acid Change
XR_940691.1:n.341-110T>A
XR_940691.3:n.233-110T>A