Canonical Allele Identifier: CA2060730569
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1869980164

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715190G>A , CM000674.2:g.105715190G>A GRCh38
NC_000012.11:g.106108968G>A , CM000674.1:g.106108968G>A GRCh37
NC_000012.10:g.104633098G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+10934G>A
NR_110109.1:n.83G>A
NR_110110.1:n.83+8334G>A
NR_110111.1:n.83+8334G>A
NR_110111.2:n.83+8334G>A