Canonical Allele Identifier: CA951438549
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1869979644

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715173T>C , CM000674.2:g.105715173T>C GRCh38
NC_000012.11:g.106108951T>C , CM000674.1:g.106108951T>C GRCh37
NC_000012.10:g.104633081T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+10917T>C
NR_110109.1:n.66T>C
NR_110110.1:n.83+8317T>C
NR_110111.1:n.83+8317T>C
NR_110111.2:n.83+8317T>C