Canonical Allele Identifier: CA1984668754
Gene: GAB2 HGNC NCBI

Linked Data

dbSNP Id: rs1856679986

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78380213dup , CM000673.2:g.78380213dup GRCh38
NC_000011.9:g.78091259dup , CM000673.1:g.78091259dup GRCh37
NC_000011.8:g.77768907dup NCBI36
NG_016171.1:g.42610dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000361507.5:c.75+37433dup MANE Select ENSP00000354952.4:n.75+37433dup
ENST00000361507.4:c.75+37433dup ENSP00000354952.4:n.75+37433dup
ENST00000526030.1:n.177+37433dup
ENST00000528886.5:c.-40+38024dup ENSP00000433762.1:n.-40+38024dup
ENST00000530915.1:c.-127-16110dup ENSP00000431868.1:n.-127-16110dup
ENST00000534823.1:n.126+37433dup
NM_080491.2:c.75+37433dup NP_536739.1:n.75+37433dup
XM_006718753.1:c.-127-16110dup XP_006718816.1:n.-127-16110dup
XM_006718753.2:c.-127-16110dup XP_006718816.1:n.-127-16110dup
NM_080491.3:c.75+37433dup MANE Select NP_536739.1:n.75+37433dup