Canonical Allele Identifier: CA683048860
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1176363336
MyVariant Identifiers: chr12:g.106109106A>G (hg19) chr12:g.105715328A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715328A>G , CM000674.2:g.105715328A>G GRCh38
NC_000012.11:g.106109106A>G , CM000674.1:g.106109106A>G GRCh37
NC_000012.10:g.104633236A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+11072A>G
NR_110109.1:n.112+109A>G
NR_110110.1:n.83+8472A>G
NR_110111.1:n.83+8472A>G
NR_110111.2:n.83+8472A>G
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