Canonical Allele Identifier: CA294443021
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1044526451

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71129387T>C , CM000679.2:g.71129387T>C GRCh38
NC_000017.10:g.69125528T>C , CM000679.1:g.69125528T>C GRCh37
NC_000017.9:g.66637123T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.217+3003A>G