Canonical Allele Identifier: CA744010571

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3667731A>T , CM000682.2:g.3667731A>T	GRCh38
NC_000020.10:g.3648378A>T , CM000682.1:g.3648378A>T	GRCh37
NC_000020.9:g.3596378A>T	NCBI36