Canonical Allele Identifier: CA607493518

Gene: CASC18

Linked Data

• dbSNP Id: rs1267886496
• gnomAD v2: 12-106108877-T-C
• gnomAD v3: 12-105715099-T-C
• gnomAD v4: 12-105715099-T-C
• MyVariant Identifiers: chr12:g.106108877T>C (hg19) ; chr12:g.105715099T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.105715099T>C , CM000674.2:g.105715099T>C	GRCh38
NC_000012.11:g.106108877T>C , CM000674.1:g.106108877T>C	GRCh37
NC_000012.10:g.104633007T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110108.1:n.54+10843T>C
NR_110109.1:n.55-63T>C
NR_110110.1:n.83+8243T>C
NR_110111.1:n.83+8243T>C
NR_110111.2:n.83+8243T>C