Canonical Allele Identifier: CA15589203
Gene: DAB2IP HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs7025486

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.121660124G>A , CM000671.2:g.121660124G>A GRCh38
NC_000009.11:g.124422403G>A , CM000671.1:g.124422403G>A GRCh37
NC_000009.10:g.123462224G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_032552.3:c.41-18554G>A VV NP_115941.2:p.=
XM_005251719.3:c.124+8225G>A XP_005251776.1:p.=
XM_005251721.1:c.41-18554G>A XP_005251778.1:p.=
XM_011518264.1:c.104-18554G>A XP_011516566.1:p.=
XM_011518265.1:c.104-18554G>A XP_011516567.1:p.=
XM_011518266.1:c.104-18554G>A XP_011516568.1:p.=
XM_011518267.1:c.104-18554G>A XP_011516569.1:p.=
XM_011518268.1:c.104-18554G>A XP_011516570.1:p.=
XM_005251719.4:c.124+8225G>A
XM_011518264.3:c.104-18554G>A
XM_011518265.3:c.104-18554G>A
XM_011518266.2:c.104-18554G>A
XM_011518267.2:c.104-18554G>A
XM_024447418.1:c.-68-18554G>A XP_024303186.1:p.=
ENST00000259371.6:c.41-18554G>A ENSP00000259371.2:p.=
ENST00000394340.7:c.41-18554G>A ENSP00000377872.3:p.=
ENST00000408936.7:c.124+8225G>A ENSP00000386183.3:p.=
ENST00000436835.5:c.-114-18554G>A ENSP00000409327.1:p.=
ENST00000465078.1:n.215+8225G>A
ENST00000489314.1:n.360-18554G>A