Canonical Allele Identifier: CA778969479

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.37634043A>T , CM000680.2:g.37634043A>T	GRCh38
NC_000018.9:g.35214006A>T , CM000680.1:g.35214006A>T	GRCh37
NC_000018.8:g.33468004A>T	NCBI36