Canonical Allele Identifier: CA2060730539
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1213618538
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715135T>A , CM000674.2:g.105715135T>A GRCh38
NC_000012.11:g.106108913T>A , CM000674.1:g.106108913T>A GRCh37
NC_000012.10:g.104633043T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+10879T>A
NR_110109.1:n.55-27T>A
NR_110110.1:n.83+8279T>A
NR_110111.1:n.83+8279T>A
NR_110111.2:n.83+8279T>A
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