Canonical Allele Identifier: CA1984668706
Gene: GAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78380091A= , CM000673.2:g.78380091A= GRCh38
NC_000011.9:g.78091137A= , CM000673.1:g.78091137A= GRCh37
NC_000011.8:g.77768785A= NCBI36
NG_016171.1:g.42732T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361507.5:c.75+37555T= MANE Select ENSP00000354952.4:n.75+37555T=
ENST00000361507.4:c.75+37555T= ENSP00000354952.4:n.75+37555T=
ENST00000526030.1:n.177+37555T=
ENST00000528886.5:c.-40+38146T= ENSP00000433762.1:n.-40+38146T=
ENST00000530915.1:c.-127-15988T= ENSP00000431868.1:n.-127-15988T=
ENST00000534823.1:n.126+37555T=
NM_080491.2:c.75+37555T= NP_536739.1:n.75+37555T=
XM_006718753.1:c.-127-15988T= XP_006718816.1:n.-127-15988T=
XM_006718753.2:c.-127-15988T= XP_006718816.1:n.-127-15988T=
NM_080491.3:c.75+37555T= MANE Select NP_536739.1:n.75+37555T=