Canonical Allele Identifier: CA200076435

Gene: DAB2IP

Linked Data

• dbSNP Id: rs570426749
• gnomAD v3: 9-121660177-T-G
• gnomAD v4: 9-121660177-T-G
• MyVariant Identifiers: chr9:g.124422456T>G (hg19) ; chr9:g.121660177T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.121660177T>G , CM000671.2:g.121660177T>G	GRCh38
NC_000009.11:g.124422456T>G , CM000671.1:g.124422456T>G	GRCh37
NC_000009.10:g.123462277T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000408936.8:c.124+8278T>G MANE Select	ENSP00000386183.3:n.124+8278T>G
ENST00000259371.7:c.41-18501T>G	ENSP00000259371.2:n.41-18501T>G
ENST00000436835.6:c.41-18501T>G	ENSP00000409327.2:n.41-18501T>G
ENST00000259371.6:c.41-18501T>G	ENSP00000259371.2:n.41-18501T>G
ENST00000394340.7:c.41-18501T>G	ENSP00000377872.3:n.41-18501T>G
ENST00000408936.7:c.124+8278T>G	ENSP00000386183.3:n.124+8278T>G
ENST00000436835.5:c.-114-18501T>G	ENSP00000409327.1:n.-114-18501T>G
ENST00000465078.1:n.215+8278T>G
ENST00000489314.1:n.360-18501T>G
NM_032552.3:c.41-18501T>G	NP_115941.2:n.41-18501T>G
XM_005251719.3:c.124+8278T>G	XP_005251776.1:n.124+8278T>G
XM_005251721.1:c.41-18501T>G	XP_005251778.1:n.41-18501T>G
XM_011518264.1:c.104-18501T>G	XP_011516566.1:n.104-18501T>G
XM_011518265.1:c.104-18501T>G	XP_011516567.1:n.104-18501T>G
XM_011518266.1:c.104-18501T>G	XP_011516568.1:n.104-18501T>G
XM_011518267.1:c.104-18501T>G	XP_011516569.1:n.104-18501T>G
XM_011518268.1:c.104-18501T>G	XP_011516570.1:n.104-18501T>G
XM_005251719.4:c.124+8278T>G	XP_005251776.1:n.124+8278T>G
XM_011518264.3:c.104-18501T>G	XP_011516566.1:n.104-18501T>G
XM_011518265.3:c.104-18501T>G	XP_011516567.1:n.104-18501T>G
XM_011518266.2:c.104-18501T>G	XP_011516568.1:n.104-18501T>G
XM_011518267.2:c.104-18501T>G	XP_011516569.1:n.104-18501T>G
XM_024447418.1:c.-68-18501T>G	XP_024303186.1:n.-68-18501T>G
NM_032552.4:c.41-18501T>G	NP_115941.2:n.41-18501T>G
NM_001395010.1:c.124+8278T>G MANE Select	NP_001381939.1:n.124+8278T>G