Canonical Allele Identifier: CA607493476

Gene: CASC18

Linked Data

• dbSNP Id: rs1313149812
• gnomAD v2: 12-106108575-A-C
• MyVariant Identifiers: chr12:g.106108575A>C (hg19) ; chr12:g.105714797A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.105714797A>C , CM000674.2:g.105714797A>C	GRCh38
NC_000012.11:g.106108575A>C , CM000674.1:g.106108575A>C	GRCh37
NC_000012.10:g.104632705A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110108.1:n.54+10541A>C
NR_110109.1:n.55-365A>C
NR_110110.1:n.83+7941A>C
NR_110111.1:n.83+7941A>C
NR_110111.2:n.83+7941A>C