Canonical Allele Identifier: CA1984621007
Gene: GAB2 HGNC NCBI

Linked Data

dbSNP Id: rs1302293917

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78281884C>T , CM000673.2:g.78281884C>T GRCh38
NC_000011.9:g.77992930C>T , CM000673.1:g.77992930C>T GRCh37
NC_000011.8:g.77670578C>T NCBI36
NG_016171.1:g.140939G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361507.5:c.76-983G>A MANE Select ENSP00000354952.4:n.76-983G>A
ENST00000340149.6:c.-39-983G>A ENSP00000343959.2:n.-39-983G>A
ENST00000361507.4:c.76-983G>A ENSP00000354952.4:n.76-983G>A
ENST00000526030.1:n.255-983G>A
ENST00000528886.5:c.-39-983G>A ENSP00000433762.1:n.-39-983G>A
ENST00000530915.1:c.-39-983G>A ENSP00000431868.1:n.-39-983G>A
ENST00000534823.1:n.127-983G>A
NM_012296.3:c.-39-983G>A NP_036428.1:n.-39-983G>A
NM_080491.2:c.76-983G>A NP_536739.1:n.76-983G>A
XM_006718753.1:c.-39-983G>A XP_006718816.1:n.-39-983G>A
XM_011545408.1:c.-341-983G>A XP_011543710.1:n.-341-983G>A
XM_006718753.2:c.-39-983G>A XP_006718816.1:n.-39-983G>A
XM_011545408.3:c.-341-983G>A XP_011543710.1:n.-341-983G>A
XM_024448782.1:c.22-983G>A XP_024304550.1:n.22-983G>A
NM_080491.3:c.76-983G>A MANE Select NP_536739.1:n.76-983G>A
NM_012296.4:c.-39-983G>A NP_036428.1:n.-39-983G>A