Canonical Allele Identifier: CA243295500
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1043365951
gnomAD v3: 12-105714778-C-G
gnomAD v4: 12-105714778-C-G
MyVariant Identifiers: chr12:g.106108556C>G (hg19) chr12:g.105714778C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105714778C>G , CM000674.2:g.105714778C>G GRCh38
NC_000012.11:g.106108556C>G , CM000674.1:g.106108556C>G GRCh37
NC_000012.10:g.104632686C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110108.1:n.54+10522C>G
NR_110109.1:n.55-384C>G
NR_110110.1:n.83+7922C>G
NR_110111.1:n.83+7922C>G
NR_110111.2:n.83+7922C>G
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