Canonical Allele Identifier: CA683048527
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1489925683
gnomAD v3: 12-105714832-A-C
gnomAD v4: 12-105714832-A-C
MyVariant Identifiers: chr12:g.106108610A>C (hg19) chr12:g.105714832A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105714832A>C , CM000674.2:g.105714832A>C GRCh38
NC_000012.11:g.106108610A>C , CM000674.1:g.106108610A>C GRCh37
NC_000012.10:g.104632740A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110108.1:n.54+10576A>C
NR_110109.1:n.55-330A>C
NR_110110.1:n.83+7976A>C
NR_110111.1:n.83+7976A>C
NR_110111.2:n.83+7976A>C
Search 100 bp 5'
Search 100 bp 3'