Canonical Allele Identifier: CA607493473

Gene: CASC18

Linked Data

• dbSNP Id: rs1222538974
• gnomAD v2: 12-106108551-A-G
• gnomAD v3: 12-105714773-A-G
• gnomAD v4: 12-105714773-A-G
• MyVariant Identifiers: chr12:g.106108551A>G (hg19) ; chr12:g.105714773A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.105714773A>G , CM000674.2:g.105714773A>G	GRCh38
NC_000012.11:g.106108551A>G , CM000674.1:g.106108551A>G	GRCh37
NC_000012.10:g.104632681A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110108.1:n.54+10517A>G
NR_110109.1:n.55-389A>G
NR_110110.1:n.83+7917A>G
NR_110111.1:n.83+7917A>G
NR_110111.2:n.83+7917A>G