Canonical Allele Identifier: CA2060730427
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1869969571

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105714848C>T , CM000674.2:g.105714848C>T GRCh38
NC_000012.11:g.106108626C>T , CM000674.1:g.106108626C>T GRCh37
NC_000012.10:g.104632756C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110108.1:n.54+10592C>T
NR_110109.1:n.55-314C>T
NR_110110.1:n.83+7992C>T
NR_110111.1:n.83+7992C>T
NR_110111.2:n.83+7992C>T