Canonical Allele Identifier: CA590477949

Gene: DAB2IP

Linked Data

• dbSNP Id: rs555996
• gnomAD v2: 9-124396311-C-A
• gnomAD v3: 9-121634032-C-A
• gnomAD v4: 9-121634032-C-A
• MyVariant Identifiers: chr9:g.124396311C>A (hg19) ; chr9:g.121634032C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.121634032C>A , CM000671.2:g.121634032C>A	GRCh38
NC_000009.11:g.124396311C>A , CM000671.1:g.124396311C>A	GRCh37
NC_000009.10:g.123436132C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000259371.7:c.41-44646C>A	ENSP00000259371.2:n.41-44646C>A
ENST00000436835.6:c.41-44646C>A	ENSP00000409327.2:n.41-44646C>A
ENST00000259371.6:c.41-44646C>A	ENSP00000259371.2:n.41-44646C>A
ENST00000394340.7:c.41-44646C>A	ENSP00000377872.3:n.41-44646C>A
ENST00000436835.5:c.-114-44646C>A	ENSP00000409327.1:n.-114-44646C>A
ENST00000489314.1:n.359+35406C>A
NM_032552.3:c.41-44646C>A	NP_115941.2:n.41-44646C>A
XM_005251721.1:c.41-44646C>A	XP_005251778.1:n.41-44646C>A
XM_011518264.1:c.103+35406C>A	XP_011516566.1:n.103+35406C>A
XM_011518265.1:c.103+35406C>A	XP_011516567.1:n.103+35406C>A
XM_011518266.1:c.103+35406C>A	XP_011516568.1:n.103+35406C>A
XM_011518267.1:c.103+35406C>A	XP_011516569.1:n.103+35406C>A
XM_011518268.1:c.103+35406C>A	XP_011516570.1:n.103+35406C>A
XM_011518264.3:c.103+35406C>A	XP_011516566.1:n.103+35406C>A
XM_011518265.3:c.103+35406C>A	XP_011516567.1:n.103+35406C>A
XM_011518266.2:c.103+35406C>A	XP_011516568.1:n.103+35406C>A
XM_011518267.2:c.103+35406C>A	XP_011516569.1:n.103+35406C>A
XM_024447418.1:c.-69+34266C>A	XP_024303186.1:n.-69+34266C>A
NM_032552.4:c.41-44646C>A	NP_115941.2:n.41-44646C>A