Canonical Allele Identifier: CA2963855238
Gene: CASC17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112516C>T , CM000679.2:g.71112516C>T GRCh38
NC_000017.10:g.69108657C>T , CM000679.1:g.69108657C>T GRCh37
NC_000017.9:g.66620252C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104152.1:n.218-12898G>A