Canonical Allele Identifier: CA985983328
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1907988859

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112669G>A , CM000679.2:g.71112669G>A GRCh38
NC_000017.10:g.69108810G>A , CM000679.1:g.69108810G>A GRCh37
NC_000017.9:g.66620405G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.218-13051C>T