Canonical Allele Identifier: CA1984668658
Gene: GAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78379988A= , CM000673.2:g.78379988A= GRCh38
NC_000011.9:g.78091034A= , CM000673.1:g.78091034A= GRCh37
NC_000011.8:g.77768682A= NCBI36
NG_016171.1:g.42835T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361507.5:c.75+37658T= MANE Select ENSP00000354952.4:n.75+37658T=
ENST00000361507.4:c.75+37658T= ENSP00000354952.4:n.75+37658T=
ENST00000526030.1:n.177+37658T=
ENST00000528886.5:c.-40+38249T= ENSP00000433762.1:n.-40+38249T=
ENST00000530915.1:c.-127-15885T= ENSP00000431868.1:n.-127-15885T=
ENST00000534823.1:n.126+37658T=
NM_080491.2:c.75+37658T= NP_536739.1:n.75+37658T=
XM_006718753.1:c.-127-15885T= XP_006718816.1:n.-127-15885T=
XM_006718753.2:c.-127-15885T= XP_006718816.1:n.-127-15885T=
NM_080491.3:c.75+37658T= MANE Select NP_536739.1:n.75+37658T=