Canonical Allele Identifier: CA774666384
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1318277411

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112647A>G , CM000679.2:g.71112647A>G GRCh38
NC_000017.10:g.69108788A>G , CM000679.1:g.69108788A>G GRCh37
NC_000017.9:g.66620383A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.218-13029T>C