Canonical Allele Identifier: CA607493509

Gene: CASC18

Linked Data

• dbSNP Id: rs1322339705
• gnomAD v2: 12-106108771-G-A
• gnomAD v3: 12-105714993-G-A
• gnomAD v4: 12-105714993-G-A
• MyVariant Identifiers: chr12:g.106108771G>A (hg19) ; chr12:g.105714993G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.105714993G>A , CM000674.2:g.105714993G>A	GRCh38
NC_000012.11:g.106108771G>A , CM000674.1:g.106108771G>A	GRCh37
NC_000012.10:g.104632901G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110108.1:n.54+10737G>A
NR_110109.1:n.55-169G>A
NR_110110.1:n.83+8137G>A
NR_110111.1:n.83+8137G>A
NR_110111.2:n.83+8137G>A