Canonical Allele Identifier: CA1984668742
Gene: GAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78380166C= , CM000673.2:g.78380166C= GRCh38
NC_000011.9:g.78091212C= , CM000673.1:g.78091212C= GRCh37
NC_000011.8:g.77768860C= NCBI36
NG_016171.1:g.42657G=

Transcript Alleles

HGVS Amino-acid change
ENST00000361507.5:c.75+37480G= MANE Select ENSP00000354952.4:n.75+37480G=
ENST00000361507.4:c.75+37480G= ENSP00000354952.4:n.75+37480G=
ENST00000526030.1:n.177+37480G=
ENST00000528886.5:c.-40+38071G= ENSP00000433762.1:n.-40+38071G=
ENST00000530915.1:c.-127-16063G= ENSP00000431868.1:n.-127-16063G=
ENST00000534823.1:n.126+37480G=
NM_080491.2:c.75+37480G= NP_536739.1:n.75+37480G=
XM_006718753.1:c.-127-16063G= XP_006718816.1:n.-127-16063G=
XM_006718753.2:c.-127-16063G= XP_006718816.1:n.-127-16063G=
NM_080491.3:c.75+37480G= MANE Select NP_536739.1:n.75+37480G=