Canonical Allele Identifier: CA2060730598
Gene: CASC18 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715243A= , CM000674.2:g.105715243A= GRCh38
NC_000012.11:g.106109021A= , CM000674.1:g.106109021A= GRCh37
NC_000012.10:g.104633151A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+10987A=
NR_110109.1:n.112+24A=
NR_110110.1:n.83+8387A=
NR_110111.1:n.83+8387A=
NR_110111.2:n.83+8387A=