Canonical Allele Identifier: CA1984650264
Gene: GAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78342103C= , CM000673.2:g.78342103C= GRCh38
NC_000011.9:g.78053149C= , CM000673.1:g.78053149C= GRCh37
NC_000011.8:g.77730797C= NCBI36
NG_016171.1:g.80720G=

Transcript Alleles

HGVS Amino-acid change
ENST00000361507.5:c.76-61202G= MANE Select ENSP00000354952.4:n.76-61202G=
ENST00000361507.4:c.76-61202G= ENSP00000354952.4:n.76-61202G=
ENST00000526030.1:n.178-23884G=
ENST00000528886.5:c.-39-61202G= ENSP00000433762.1:n.-39-61202G=
ENST00000530915.1:c.-40+21913G= ENSP00000431868.1:n.-40+21913G=
ENST00000534823.1:n.127-61202G=
NM_080491.2:c.76-61202G= NP_536739.1:n.76-61202G=
XM_006718753.1:c.-40+21913G= XP_006718816.1:n.-40+21913G=
XM_006718753.2:c.-40+21913G= XP_006718816.1:n.-40+21913G=
XM_024448782.1:c.21+12631G= XP_024304550.1:n.21+12631G=
NM_080491.3:c.76-61202G= MANE Select NP_536739.1:n.76-61202G=