Canonical Allele Identifier: CA607493482

Gene: CASC18

Linked Data

• dbSNP Id: rs1468582197
• gnomAD v2: 12-106108653-C-T
• gnomAD v3: 12-105714875-C-T
• gnomAD v4: 12-105714875-C-T
• MyVariant Identifiers: chr12:g.106108653C>T (hg19) ; chr12:g.105714875C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.105714875C>T , CM000674.2:g.105714875C>T	GRCh38
NC_000012.11:g.106108653C>T , CM000674.1:g.106108653C>T	GRCh37
NC_000012.10:g.104632783C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110108.1:n.54+10619C>T
NR_110109.1:n.55-287C>T
NR_110110.1:n.83+8019C>T
NR_110111.1:n.83+8019C>T
NR_110111.2:n.83+8019C>T