Canonical Allele Identifier: CA1984650268
Gene: GAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78342111G= , CM000673.2:g.78342111G= GRCh38
NC_000011.9:g.78053157G= , CM000673.1:g.78053157G= GRCh37
NC_000011.8:g.77730805G= NCBI36
NG_016171.1:g.80712C=

Transcript Alleles

HGVS Amino-acid change
ENST00000361507.5:c.76-61210C= MANE Select ENSP00000354952.4:n.76-61210C=
ENST00000361507.4:c.76-61210C= ENSP00000354952.4:n.76-61210C=
ENST00000526030.1:n.178-23892C=
ENST00000528886.5:c.-39-61210C= ENSP00000433762.1:n.-39-61210C=
ENST00000530915.1:c.-40+21905C= ENSP00000431868.1:n.-40+21905C=
ENST00000534823.1:n.127-61210C=
NM_080491.2:c.76-61210C= NP_536739.1:n.76-61210C=
XM_006718753.1:c.-40+21905C= XP_006718816.1:n.-40+21905C=
XM_006718753.2:c.-40+21905C= XP_006718816.1:n.-40+21905C=
XM_024448782.1:c.21+12623C= XP_024304550.1:n.21+12623C=
NM_080491.3:c.76-61210C= MANE Select NP_536739.1:n.76-61210C=