Canonical Allele Identifier: CA774666227
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1394264946

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112398T>C , CM000679.2:g.71112398T>C GRCh38
NC_000017.10:g.69108539T>C , CM000679.1:g.69108539T>C GRCh37
NC_000017.9:g.66620134T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104152.1:n.218-12780A>G