Canonical Allele Identifier: CA683048669
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1320923248
gnomAD v3: 12-105715032-T-C
gnomAD v4: 12-105715032-T-C
MyVariant Identifiers: chr12:g.106108810T>C (hg19) chr12:g.105715032T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715032T>C , CM000674.2:g.105715032T>C GRCh38
NC_000012.11:g.106108810T>C , CM000674.1:g.106108810T>C GRCh37
NC_000012.10:g.104632940T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+10776T>C
NR_110109.1:n.55-130T>C
NR_110110.1:n.83+8176T>C
NR_110111.1:n.83+8176T>C
NR_110111.2:n.83+8176T>C
Search 100 bp 5'
Search 100 bp 3'