Canonical Allele Identifier: CA904021834

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.188022735T>G , CM000665.2:g.188022735T>G	GRCh38
NC_000003.11:g.187740523T>G , CM000665.1:g.187740523T>G	GRCh37
NC_000003.10:g.189223217T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001741061.1:n.163-18747A>C