Canonical Allele Identifier: CA1984668705
Gene: GAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78380089G= , CM000673.2:g.78380089G= GRCh38
NC_000011.9:g.78091135G= , CM000673.1:g.78091135G= GRCh37
NC_000011.8:g.77768783G= NCBI36
NG_016171.1:g.42734C=

Transcript Alleles

HGVS Amino-acid change
ENST00000361507.5:c.75+37557C= MANE Select ENSP00000354952.4:n.75+37557C=
ENST00000361507.4:c.75+37557C= ENSP00000354952.4:n.75+37557C=
ENST00000526030.1:n.177+37557C=
ENST00000528886.5:c.-40+38148C= ENSP00000433762.1:n.-40+38148C=
ENST00000530915.1:c.-127-15986C= ENSP00000431868.1:n.-127-15986C=
ENST00000534823.1:n.126+37557C=
NM_080491.2:c.75+37557C= NP_536739.1:n.75+37557C=
XM_006718753.1:c.-127-15986C= XP_006718816.1:n.-127-15986C=
XM_006718753.2:c.-127-15986C= XP_006718816.1:n.-127-15986C=
NM_080491.3:c.75+37557C= MANE Select NP_536739.1:n.75+37557C=