Canonical Allele Identifier: CA15620719

Gene: DAB2IP

Linked Data

• dbSNP Id: rs1571801
• gnomAD: 9:124427373 G / T
• MyVariant Identifiers: chr9:g.124427373G>T (hg19) ; chr9:g.121665094G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.121665094G>T , CM000671.2:g.121665094G>T	GRCh38
NC_000009.11:g.124427373G>T , CM000671.1:g.124427373G>T	GRCh37
NC_000009.10:g.123467194G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000259371.6:c.41-13584G>T	ENSP00000259371.2:p.=
ENST00000394340.7:c.41-13584G>T	ENSP00000377872.3:p.=
ENST00000408936.7:c.124+13195G>T	ENSP00000386183.3:p.=
ENST00000436835.5:c.-114-13584G>T	ENSP00000409327.1:p.=
NM_032552.3:c.41-13584G>T	NP_115941.2:p.=
XM_005251719.3:c.124+13195G>T	XP_005251776.1:p.=
XM_005251721.1:c.41-13584G>T	XP_005251778.1:p.=
XM_011518264.1:c.104-13584G>T	XP_011516566.1:p.=
XM_011518265.1:c.104-13584G>T	XP_011516567.1:p.=
XM_011518266.1:c.104-13584G>T	XP_011516568.1:p.=
XM_011518267.1:c.104-13584G>T	XP_011516569.1:p.=
XM_011518268.1:c.104-13584G>T	XP_011516570.1:p.=
XM_005251719.4:c.124+13195G>T	XP_005251776.1:p.=
XM_011518264.3:c.104-13584G>T	XP_011516566.1:p.=
XM_011518265.3:c.104-13584G>T	XP_011516567.1:p.=
XM_011518266.2:c.104-13584G>T	XP_011516568.1:p.=
XM_011518267.2:c.104-13584G>T	XP_011516569.1:p.=
XM_024447418.1:c.-68-13584G>T	XP_024303186.1:p.=
NM_032552.4:c.41-13584G>T	NP_115941.2:p.=