Canonical Allele Identifier: CA243295653
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1034600173
gnomAD v3: 12-105715281-T-G
gnomAD v4: 12-105715281-T-G
MyVariant Identifiers: chr12:g.106109059T>G (hg19) chr12:g.105715281T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715281T>G , CM000674.2:g.105715281T>G GRCh38
NC_000012.11:g.106109059T>G , CM000674.1:g.106109059T>G GRCh37
NC_000012.10:g.104633189T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+11025T>G
NR_110109.1:n.112+62T>G
NR_110110.1:n.83+8425T>G
NR_110111.1:n.83+8425T>G
NR_110111.2:n.83+8425T>G
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