Canonical Allele Identifier: CA774666268
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1271514697

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112469C>T , CM000679.2:g.71112469C>T GRCh38
NC_000017.10:g.69108610C>T , CM000679.1:g.69108610C>T GRCh37
NC_000017.9:g.66620205C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.218-12851G>A