Canonical Allele Identifier: CA746603039

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.6629230G>C , CM000682.2:g.6629230G>C	GRCh38
NC_000020.10:g.6609877G>C , CM000682.1:g.6609877G>C	GRCh37
NC_000020.9:g.6557877G>C	NCBI36