Canonical Allele Identifier: CA774666357
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs146356533

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112609G>T , CM000679.2:g.71112609G>T GRCh38
NC_000017.10:g.69108750G>T , CM000679.1:g.69108750G>T GRCh37
NC_000017.9:g.66620345G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.218-12991C>A