Canonical Allele Identifier: CA774666390

Gene: CASC17

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.71112656A>C , CM000679.2:g.71112656A>C	GRCh38
NC_000017.10:g.69108797A>C , CM000679.1:g.69108797A>C	GRCh37
NC_000017.9:g.66620392A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_104152.1:n.218-13038T>G