Canonical Allele Identifier: CA215030469

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.117586350A>C , CM000672.2:g.117586350A>C	GRCh38
NC_000010.10:g.119345861A>C , CM000672.1:g.119345861A>C	GRCh37
NC_000010.9:g.119335851A>C	NCBI36