Canonical Allele Identifier: CA683048709

Gene: CASC18

Linked Data

• dbSNP Id: rs1362102516
• gnomAD v3: 12-105715138-G-C
• gnomAD v4: 12-105715138-G-C
• MyVariant Identifiers: chr12:g.106108916G>C (hg19) ; chr12:g.105715138G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.105715138G>C , CM000674.2:g.105715138G>C	GRCh38
NC_000012.11:g.106108916G>C , CM000674.1:g.106108916G>C	GRCh37
NC_000012.10:g.104633046G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110108.1:n.54+10882G>C
NR_110109.1:n.55-24G>C
NR_110110.1:n.83+8282G>C
NR_110111.1:n.83+8282G>C
NR_110111.2:n.83+8282G>C