Canonical Allele Identifier: CA1984650285
Gene: GAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78342146T= , CM000673.2:g.78342146T= GRCh38
NC_000011.9:g.78053192T= , CM000673.1:g.78053192T= GRCh37
NC_000011.8:g.77730840T= NCBI36
NG_016171.1:g.80677A=

Transcript Alleles

HGVS Amino-acid change
ENST00000361507.5:c.76-61245A= MANE Select ENSP00000354952.4:n.76-61245A=
ENST00000361507.4:c.76-61245A= ENSP00000354952.4:n.76-61245A=
ENST00000526030.1:n.178-23927A=
ENST00000528886.5:c.-39-61245A= ENSP00000433762.1:n.-39-61245A=
ENST00000530915.1:c.-40+21870A= ENSP00000431868.1:n.-40+21870A=
ENST00000534823.1:n.127-61245A=
NM_080491.2:c.76-61245A= NP_536739.1:n.76-61245A=
XM_006718753.1:c.-40+21870A= XP_006718816.1:n.-40+21870A=
XM_006718753.2:c.-40+21870A= XP_006718816.1:n.-40+21870A=
XM_024448782.1:c.21+12588A= XP_024304550.1:n.21+12588A=
NM_080491.3:c.76-61245A= MANE Select NP_536739.1:n.76-61245A=