Canonical Allele Identifier: CA2060730498
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1565858385

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715022T>C , CM000674.2:g.105715022T>C GRCh38
NC_000012.11:g.106108800T>C , CM000674.1:g.106108800T>C GRCh37
NC_000012.10:g.104632930T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110108.1:n.54+10766T>C
NR_110109.1:n.55-140T>C
NR_110110.1:n.83+8166T>C
NR_110111.1:n.83+8166T>C
NR_110111.2:n.83+8166T>C