Canonical Allele Identifier: CA669979609

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92451547C>A , CM000672.2:g.92451547C>A	GRCh38
NC_000010.10:g.94211304C>A , CM000672.1:g.94211304C>A	GRCh37
NC_000010.9:g.94201284C>A	NCBI36
NG_013012.1:g.127549G>T