Canonical Allele Identifier: CA889387811

Gene: CCDST

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152205542C>T , CM000663.2:g.152205542C>T	GRCh38
NC_000001.10:g.152178018C>T , CM000663.1:g.152178018C>T	GRCh37
NC_000001.9:g.150444642C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_002958366.1:n.936-318C>T