Canonical Allele Identifier: CA1984668661
Gene: GAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78379994A= , CM000673.2:g.78379994A= GRCh38
NC_000011.9:g.78091040A= , CM000673.1:g.78091040A= GRCh37
NC_000011.8:g.77768688A= NCBI36
NG_016171.1:g.42829T=

Transcript Alleles

HGVS Amino-acid change
ENST00000361507.5:c.75+37652T= MANE Select ENSP00000354952.4:n.75+37652T=
ENST00000361507.4:c.75+37652T= ENSP00000354952.4:n.75+37652T=
ENST00000526030.1:n.177+37652T=
ENST00000528886.5:c.-40+38243T= ENSP00000433762.1:n.-40+38243T=
ENST00000530915.1:c.-127-15891T= ENSP00000431868.1:n.-127-15891T=
ENST00000534823.1:n.126+37652T=
NM_080491.2:c.75+37652T= NP_536739.1:n.75+37652T=
XM_006718753.1:c.-127-15891T= XP_006718816.1:n.-127-15891T=
XM_006718753.2:c.-127-15891T= XP_006718816.1:n.-127-15891T=
NM_080491.3:c.75+37652T= MANE Select NP_536739.1:n.75+37652T=