Canonical Allele Identifier: CA1984668636
Gene: GAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78379949T= , CM000673.2:g.78379949T= GRCh38
NC_000011.9:g.78090995T= , CM000673.1:g.78090995T= GRCh37
NC_000011.8:g.77768643T= NCBI36
NG_016171.1:g.42874A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361507.5:c.75+37697A= MANE Select ENSP00000354952.4:n.75+37697A=
ENST00000361507.4:c.75+37697A= ENSP00000354952.4:n.75+37697A=
ENST00000526030.1:n.177+37697A=
ENST00000528886.5:c.-40+38288A= ENSP00000433762.1:n.-40+38288A=
ENST00000530915.1:c.-127-15846A= ENSP00000431868.1:n.-127-15846A=
ENST00000534823.1:n.126+37697A=
NM_080491.2:c.75+37697A= NP_536739.1:n.75+37697A=
XM_006718753.1:c.-127-15846A= XP_006718816.1:n.-127-15846A=
XM_006718753.2:c.-127-15846A= XP_006718816.1:n.-127-15846A=
NM_080491.3:c.75+37697A= MANE Select NP_536739.1:n.75+37697A=