Canonical Allele Identifier: CA1984668758
Gene: GAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78380217T= , CM000673.2:g.78380217T= GRCh38
NC_000011.9:g.78091263T= , CM000673.1:g.78091263T= GRCh37
NC_000011.8:g.77768911T= NCBI36
NG_016171.1:g.42606A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361507.5:c.75+37429A= MANE Select ENSP00000354952.4:n.75+37429A=
ENST00000361507.4:c.75+37429A= ENSP00000354952.4:n.75+37429A=
ENST00000526030.1:n.177+37429A=
ENST00000528886.5:c.-40+38020A= ENSP00000433762.1:n.-40+38020A=
ENST00000530915.1:c.-127-16114A= ENSP00000431868.1:n.-127-16114A=
ENST00000534823.1:n.126+37429A=
NM_080491.2:c.75+37429A= NP_536739.1:n.75+37429A=
XM_006718753.1:c.-127-16114A= XP_006718816.1:n.-127-16114A=
XM_006718753.2:c.-127-16114A= XP_006718816.1:n.-127-16114A=
NM_080491.3:c.75+37429A= MANE Select NP_536739.1:n.75+37429A=