Canonical Allele Identifier: CA1984650263
Gene: GAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78342102A= , CM000673.2:g.78342102A= GRCh38
NC_000011.9:g.78053148A= , CM000673.1:g.78053148A= GRCh37
NC_000011.8:g.77730796A= NCBI36
NG_016171.1:g.80721T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361507.5:c.76-61201T= MANE Select ENSP00000354952.4:n.76-61201T=
ENST00000361507.4:c.76-61201T= ENSP00000354952.4:n.76-61201T=
ENST00000526030.1:n.178-23883T=
ENST00000528886.5:c.-39-61201T= ENSP00000433762.1:n.-39-61201T=
ENST00000530915.1:c.-40+21914T= ENSP00000431868.1:n.-40+21914T=
ENST00000534823.1:n.127-61201T=
NM_080491.2:c.76-61201T= NP_536739.1:n.76-61201T=
XM_006718753.1:c.-40+21914T= XP_006718816.1:n.-40+21914T=
XM_006718753.2:c.-40+21914T= XP_006718816.1:n.-40+21914T=
XM_024448782.1:c.21+12632T= XP_024304550.1:n.21+12632T=
NM_080491.3:c.76-61201T= MANE Select NP_536739.1:n.76-61201T=