Canonical Allele Identifier: CA243295612
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs983949597
gnomAD v2: 12-106108993-A-G
gnomAD v3: 12-105715215-A-G
gnomAD v4: 12-105715215-A-G
MyVariant Identifiers: chr12:g.106108993A>G (hg19) chr12:g.105715215A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715215A>G , CM000674.2:g.105715215A>G GRCh38
NC_000012.11:g.106108993A>G , CM000674.1:g.106108993A>G GRCh37
NC_000012.10:g.104633123A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+10959A>G
NR_110109.1:n.108A>G
NR_110110.1:n.83+8359A>G
NR_110111.1:n.83+8359A>G
NR_110111.2:n.83+8359A>G
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