Canonical Allele Identifier: CA665997101

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49353462T>G , CM000672.2:g.49353462T>G	GRCh38
NC_000010.10:g.50561507T>G , CM000672.1:g.50561507T>G	GRCh37
NC_000010.9:g.50231513T>G	NCBI36