Canonical Allele Identifier: CA516490588

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.51486835C>T , CM000685.2:g.51486835C>T	GRCh38
NC_000023.10:g.51229687C>T , CM000685.1:g.51229687C>T	GRCh37
NC_000023.9:g.51246427C>T	NCBI36