Canonical Allele Identifier: CA243295623
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs961237605
MyVariant Identifiers: chr12:g.106108998G>C (hg19) chr12:g.105715220G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715220G>C , CM000674.2:g.105715220G>C GRCh38
NC_000012.11:g.106108998G>C , CM000674.1:g.106108998G>C GRCh37
NC_000012.10:g.104633128G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+10964G>C
NR_110109.1:n.112+1G>C
NR_110110.1:n.83+8364G>C
NR_110111.1:n.83+8364G>C
NR_110111.2:n.83+8364G>C
Search 100 bp 5'
Search 100 bp 3'