Canonical Allele Identifier: CA669972896

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92705733T>C , CM000672.2:g.92705733T>C	GRCh38
NC_000010.10:g.94465490T>C , CM000672.1:g.94465490T>C	GRCh37
NC_000010.9:g.94455470T>C	NCBI36