Canonical Allele Identifier: CA607493532

Gene: CASC18

Linked Data

• dbSNP Id: rs1431084923
• gnomAD v2: 12-106109000-A-G
• gnomAD v3: 12-105715222-A-G
• gnomAD v4: 12-105715222-A-G
• MyVariant Identifiers: chr12:g.106109000A>G (hg19) ; chr12:g.105715222A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.105715222A>G , CM000674.2:g.105715222A>G	GRCh38
NC_000012.11:g.106109000A>G , CM000674.1:g.106109000A>G	GRCh37
NC_000012.10:g.104633130A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110108.1:n.54+10966A>G
NR_110109.1:n.112+3A>G
NR_110110.1:n.83+8366A>G
NR_110111.1:n.83+8366A>G
NR_110111.2:n.83+8366A>G