Canonical Allele Identifier: CA696386520

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.20162077C>T , CM000675.2:g.20162077C>T	GRCh38
NC_000013.10:g.20736216C>T , CM000675.1:g.20736216C>T	GRCh37
NC_000013.9:g.19634216C>T	NCBI36
NG_016399.1:g.3968G>A