Canonical Allele Identifier: CA673021680

Gene: CDON VSIG10L2

Linked Data

• dbSNP Id: rs1187879075
• gnomAD v2: 11-125826619-A-G
• gnomAD v3: 11-125956724-A-G
• gnomAD v4: 11-125956724-A-G
• MyVariant Identifiers: chr11:g.125826619A>G (hg19) ; chr11:g.125956724A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.125956724A>G , CM000673.2:g.125956724A>G	GRCh38
NC_000011.9:g.125826619A>G , CM000673.1:g.125826619A>G	GRCh37
NC_000011.8:g.125331829A>G	NCBI36
NG_029776.1:g.111569T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000684078.1:c.*4218T>C (CDON)	ENSP00000507318.1:n.*4218T>C
ENST00000638636.2:c.3114A>G (VSIG10L2)	ENSP00000491467.1:n.3114A>G
ENST00000392693.7:c.*4218T>C (CDON)	ENSP00000376458.3:n.*4218T>C
XM_006718950.2:c.3510A>G (VSIG10L2)	XP_006719013.2:n.3510A>G