Canonical Allele Identifier: CA1984668672
Gene: GAB2 HGNC NCBI

Linked Data

dbSNP Id: rs1856677809

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78380021T>G , CM000673.2:g.78380021T>G GRCh38
NC_000011.9:g.78091067T>G , CM000673.1:g.78091067T>G GRCh37
NC_000011.8:g.77768715T>G NCBI36
NG_016171.1:g.42802A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000361507.5:c.75+37625A>C MANE Select ENSP00000354952.4:n.75+37625A>C
ENST00000361507.4:c.75+37625A>C ENSP00000354952.4:n.75+37625A>C
ENST00000526030.1:n.177+37625A>C
ENST00000528886.5:c.-40+38216A>C ENSP00000433762.1:n.-40+38216A>C
ENST00000530915.1:c.-127-15918A>C ENSP00000431868.1:n.-127-15918A>C
ENST00000534823.1:n.126+37625A>C
NM_080491.2:c.75+37625A>C NP_536739.1:n.75+37625A>C
XM_006718753.1:c.-127-15918A>C XP_006718816.1:n.-127-15918A>C
XM_006718753.2:c.-127-15918A>C XP_006718816.1:n.-127-15918A>C
NM_080491.3:c.75+37625A>C MANE Select NP_536739.1:n.75+37625A>C