Canonical Allele Identifier: CA2060730431
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1869969805

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105714857C>T , CM000674.2:g.105714857C>T GRCh38
NC_000012.11:g.106108635C>T , CM000674.1:g.106108635C>T GRCh37
NC_000012.10:g.104632765C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110108.1:n.54+10601C>T
NR_110109.1:n.55-305C>T
NR_110110.1:n.83+8001C>T
NR_110111.1:n.83+8001C>T
NR_110111.2:n.83+8001C>T