Canonical Allele Identifier: CA2060730442
Gene: CASC18 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105714888T= , CM000674.2:g.105714888T= GRCh38
NC_000012.11:g.106108666T= , CM000674.1:g.106108666T= GRCh37
NC_000012.10:g.104632796T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110108.1:n.54+10632T=
NR_110109.1:n.55-274T=
NR_110110.1:n.83+8032T=
NR_110111.1:n.83+8032T=
NR_110111.2:n.83+8032T=