Canonical Allele Identifier: CA607493546
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1292433120
gnomAD v2: 12-106109023-A-T
gnomAD v3: 12-105715245-A-T
gnomAD v4: 12-105715245-A-T
MyVariant Identifiers: chr12:g.106109023A>T (hg19) chr12:g.105715245A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715245A>T , CM000674.2:g.105715245A>T GRCh38
NC_000012.11:g.106109023A>T , CM000674.1:g.106109023A>T GRCh37
NC_000012.10:g.104633153A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+10989A>T
NR_110109.1:n.112+26A>T
NR_110110.1:n.83+8389A>T
NR_110111.1:n.83+8389A>T
NR_110111.2:n.83+8389A>T
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