Canonical Allele Identifier: CA243295652
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs766916988
gnomAD v3: 12-105715278-A-G
gnomAD v4: 12-105715278-A-G
MyVariant Identifiers: chr12:g.106109056A>G (hg19) chr12:g.105715278A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715278A>G , CM000674.2:g.105715278A>G GRCh38
NC_000012.11:g.106109056A>G , CM000674.1:g.106109056A>G GRCh37
NC_000012.10:g.104633186A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+11022A>G
NR_110109.1:n.112+59A>G
NR_110110.1:n.83+8422A>G
NR_110111.1:n.83+8422A>G
NR_110111.2:n.83+8422A>G
Search 100 bp 5'
Search 100 bp 3'