Canonical Allele Identifier: CA735454751

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.36696751A>T , CM000663.2:g.36696751A>T	GRCh38
NC_000001.10:g.37162352A>T , CM000663.1:g.37162352A>T	GRCh37
NC_000001.9:g.36934939A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001737977.1:n.106+5465T>A