Canonical Allele Identifier: CA243295511
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs745678381
MyVariant Identifiers: chr12:g.106108612T>C (hg19) chr12:g.105714834T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105714834T>C , CM000674.2:g.105714834T>C GRCh38
NC_000012.11:g.106108612T>C , CM000674.1:g.106108612T>C GRCh37
NC_000012.10:g.104632742T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+10578T>C
NR_110109.1:n.55-328T>C
NR_110110.1:n.83+7978T>C
NR_110111.1:n.83+7978T>C
NR_110111.2:n.83+7978T>C
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