Canonical Allele Identifier: CA293056398
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1017265252

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112705G>A , CM000679.2:g.71112705G>A GRCh38
NC_000017.10:g.69108846G>A , CM000679.1:g.69108846G>A GRCh37
NC_000017.9:g.66620441G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.218-13087C>T