Canonical Allele Identifier: CA300346778

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.49001729G>T , CM000680.2:g.49001729G>T	GRCh38
NC_000018.9:g.46528099G>T , CM000680.1:g.46528099G>T	GRCh37
NC_000018.8:g.44782097G>T	NCBI36