Canonical Allele Identifier: CA951438432
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1869968018
gnomAD v3: 12-105714786-C-T
gnomAD v4: 12-105714786-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105714786C>T , CM000674.2:g.105714786C>T GRCh38
NC_000012.11:g.106108564C>T , CM000674.1:g.106108564C>T GRCh37
NC_000012.10:g.104632694C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+10530C>T
NR_110109.1:n.55-376C>T
NR_110110.1:n.83+7930C>T
NR_110111.1:n.83+7930C>T
NR_110111.2:n.83+7930C>T
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