Canonical Allele Identifier: CA774666303
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1375101052

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112508G>C , CM000679.2:g.71112508G>C GRCh38
NC_000017.10:g.69108649G>C , CM000679.1:g.69108649G>C GRCh37
NC_000017.9:g.66620244G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.218-12890C>G