Canonical Allele Identifier: CA837112683

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.26143117T>C , CM000669.2:g.26143117T>C	GRCh38
NC_000007.13:g.26182737T>C , CM000669.1:g.26182737T>C	GRCh37
NC_000007.12:g.26149262T>C	NCBI36