Canonical Allele Identifier: CA2060730572
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1869980369

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715196G>A , CM000674.2:g.105715196G>A GRCh38
NC_000012.11:g.106108974G>A , CM000674.1:g.106108974G>A GRCh37
NC_000012.10:g.104633104G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+10940G>A
NR_110109.1:n.89G>A
NR_110110.1:n.83+8340G>A
NR_110111.1:n.83+8340G>A
NR_110111.2:n.83+8340G>A