Canonical Allele Identifier: CA774666300
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1300233608

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112500C>T , CM000679.2:g.71112500C>T GRCh38
NC_000017.10:g.69108641C>T , CM000679.1:g.69108641C>T GRCh37
NC_000017.9:g.66620236C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.218-12882G>A