Canonical Allele Identifier: CA208534121

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61876772T>G , CM000672.2:g.61876772T>G	GRCh38
NC_000010.10:g.63636531T>G , CM000672.1:g.63636531T>G	GRCh37
NC_000010.9:g.63306537T>G	NCBI36