Canonical Allele Identifier: CA2060730629
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1869985216
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715307G>A , CM000674.2:g.105715307G>A GRCh38
NC_000012.11:g.106109085G>A , CM000674.1:g.106109085G>A GRCh37
NC_000012.10:g.104633215G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+11051G>A
NR_110109.1:n.112+88G>A
NR_110110.1:n.83+8451G>A
NR_110111.1:n.83+8451G>A
NR_110111.2:n.83+8451G>A
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