Canonical Allele Identifier: CA690788097

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.63154842A>C , CM000674.2:g.63154842A>C	GRCh38
NC_000012.11:g.63548622A>C , CM000674.1:g.63548622A>C	GRCh37
NC_000012.10:g.61834889A>C	NCBI36