Canonical Allele Identifier: CA1984668744
Gene: GAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78380169G= , CM000673.2:g.78380169G= GRCh38
NC_000011.9:g.78091215G= , CM000673.1:g.78091215G= GRCh37
NC_000011.8:g.77768863G= NCBI36
NG_016171.1:g.42654C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361507.5:c.75+37477C= MANE Select ENSP00000354952.4:n.75+37477C=
ENST00000361507.4:c.75+37477C= ENSP00000354952.4:n.75+37477C=
ENST00000526030.1:n.177+37477C=
ENST00000528886.5:c.-40+38068C= ENSP00000433762.1:n.-40+38068C=
ENST00000530915.1:c.-127-16066C= ENSP00000431868.1:n.-127-16066C=
ENST00000534823.1:n.126+37477C=
NM_080491.2:c.75+37477C= NP_536739.1:n.75+37477C=
XM_006718753.1:c.-127-16066C= XP_006718816.1:n.-127-16066C=
XM_006718753.2:c.-127-16066C= XP_006718816.1:n.-127-16066C=
NM_080491.3:c.75+37477C= MANE Select NP_536739.1:n.75+37477C=