Canonical Allele Identifier: CA2273435951
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1908461729

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71129385C>T , CM000679.2:g.71129385C>T GRCh38
NC_000017.10:g.69125526C>T , CM000679.1:g.69125526C>T GRCh37
NC_000017.9:g.66637121C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.217+3005G>A