Canonical Allele Identifier: CA293056164
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs532248305

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112326A>G , CM000679.2:g.71112326A>G GRCh38
NC_000017.10:g.69108467A>G , CM000679.1:g.69108467A>G GRCh37
NC_000017.9:g.66620062A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104152.1:n.218-12708T>C