Canonical Allele Identifier: CA683048862
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1480763394
gnomAD v3: 12-105715343-T-C
gnomAD v4: 12-105715343-T-C
MyVariant Identifiers: chr12:g.106109121T>C (hg19) chr12:g.105715343T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715343T>C , CM000674.2:g.105715343T>C GRCh38
NC_000012.11:g.106109121T>C , CM000674.1:g.106109121T>C GRCh37
NC_000012.10:g.104633251T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+11087T>C
NR_110109.1:n.112+124T>C
NR_110110.1:n.83+8487T>C
NR_110111.1:n.83+8487T>C
NR_110111.2:n.83+8487T>C
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