Canonical Allele Identifier: CA702777930

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.97401538G>C , CM000675.2:g.97401538G>C	GRCh38
NC_000013.10:g.98053792G>C , CM000675.1:g.98053792G>C	GRCh37
NC_000013.9:g.96851793G>C	NCBI36