Canonical Allele Identifier: CA294443025
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs543276495

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71129389G>A , CM000679.2:g.71129389G>A GRCh38
NC_000017.10:g.69125530G>A , CM000679.1:g.69125530G>A GRCh37
NC_000017.9:g.66637125G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.217+3001C>T