Canonical Allele Identifier: CA2060730556
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1592753170

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715166A>C , CM000674.2:g.105715166A>C GRCh38
NC_000012.11:g.106108944A>C , CM000674.1:g.106108944A>C GRCh37
NC_000012.10:g.104633074A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+10910A>C
NR_110109.1:n.59A>C
NR_110110.1:n.83+8310A>C
NR_110111.1:n.83+8310A>C
NR_110111.2:n.83+8310A>C