Canonical Allele Identifier: CA683048769
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1243060708
MyVariant Identifiers: chr12:g.106109007C>A (hg19) chr12:g.105715229C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715229C>A , CM000674.2:g.105715229C>A GRCh38
NC_000012.11:g.106109007C>A , CM000674.1:g.106109007C>A GRCh37
NC_000012.10:g.104633137C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+10973C>A
NR_110109.1:n.112+10C>A
NR_110110.1:n.83+8373C>A
NR_110111.1:n.83+8373C>A
NR_110111.2:n.83+8373C>A
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