Canonical Allele Identifier: CA243295497
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs946104710
gnomAD v3: 12-105714776-C-T
gnomAD v4: 12-105714776-C-T
MyVariant Identifiers: chr12:g.106108554C>T (hg19) chr12:g.105714776C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105714776C>T , CM000674.2:g.105714776C>T GRCh38
NC_000012.11:g.106108554C>T , CM000674.1:g.106108554C>T GRCh37
NC_000012.10:g.104632684C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+10520C>T
NR_110109.1:n.55-386C>T
NR_110110.1:n.83+7920C>T
NR_110111.1:n.83+7920C>T
NR_110111.2:n.83+7920C>T
Search 100 bp 5'
Search 100 bp 3'