Canonical Allele Identifier: CA2060730634
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1869985455

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715317A>C , CM000674.2:g.105715317A>C GRCh38
NC_000012.11:g.106109095A>C , CM000674.1:g.106109095A>C GRCh37
NC_000012.10:g.104633225A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+11061A>C
NR_110109.1:n.112+98A>C
NR_110110.1:n.83+8461A>C
NR_110111.1:n.83+8461A>C
NR_110111.2:n.83+8461A>C