Canonical Allele Identifier: CA2060730541
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1869978261
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715141A>T , CM000674.2:g.105715141A>T GRCh38
NC_000012.11:g.106108919A>T , CM000674.1:g.106108919A>T GRCh37
NC_000012.10:g.104633049A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+10885A>T
NR_110109.1:n.55-21A>T
NR_110110.1:n.83+8285A>T
NR_110111.1:n.83+8285A>T
NR_110111.2:n.83+8285A>T
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