Canonical Allele Identifier: CA2273435986
Gene: CASC17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71129472T= , CM000679.2:g.71129472T= GRCh38
NC_000017.10:g.69125613T= , CM000679.1:g.69125613T= GRCh37
NC_000017.9:g.66637208T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.217+2918A=