Canonical Allele Identifier: CA243295502
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs904463449
gnomAD v3: 12-105714779-C-T
gnomAD v4: 12-105714779-C-T
MyVariant Identifiers: chr12:g.106108557C>T (hg19) chr12:g.105714779C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105714779C>T , CM000674.2:g.105714779C>T GRCh38
NC_000012.11:g.106108557C>T , CM000674.1:g.106108557C>T GRCh37
NC_000012.10:g.104632687C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+10523C>T
NR_110109.1:n.55-383C>T
NR_110110.1:n.83+7923C>T
NR_110111.1:n.83+7923C>T
NR_110111.2:n.83+7923C>T
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