Canonical Allele Identifier: CA607493474

Gene: CASC18

Linked Data

• dbSNP Id: rs1306791293
• gnomAD v2: 12-106108568-C-A
• gnomAD v3: 12-105714790-C-A
• gnomAD v4: 12-105714790-C-A
• MyVariant Identifiers: chr12:g.106108568C>A (hg19) ; chr12:g.105714790C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.105714790C>A , CM000674.2:g.105714790C>A	GRCh38
NC_000012.11:g.106108568C>A , CM000674.1:g.106108568C>A	GRCh37
NC_000012.10:g.104632698C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110108.1:n.54+10534C>A
NR_110109.1:n.55-372C>A
NR_110110.1:n.83+7934C>A
NR_110111.1:n.83+7934C>A
NR_110111.2:n.83+7934C>A