Canonical Allele Identifier: CA2060730487
Gene: CASC18 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105714997A= , CM000674.2:g.105714997A= GRCh38
NC_000012.11:g.106108775A= , CM000674.1:g.106108775A= GRCh37
NC_000012.10:g.104632905A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110108.1:n.54+10741A=
NR_110109.1:n.55-165A=
NR_110110.1:n.83+8141A=
NR_110111.1:n.83+8141A=
NR_110111.2:n.83+8141A=