Canonical Allele Identifier: CA660612330

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119206827T>G , CM000672.2:g.119206827T>G	GRCh38
NC_000010.10:g.120966339T>G , CM000672.1:g.120966339T>G	GRCh37
NC_000010.9:g.120956329T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011540456.1:c.521A>C	XP_011538758.1:p.Gln174Pro