Canonical Allele Identifier: CA1984668681
Gene: GAB2 HGNC NCBI

Linked Data

dbSNP Id: rs1856678018

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78380039A>G , CM000673.2:g.78380039A>G GRCh38
NC_000011.9:g.78091085A>G , CM000673.1:g.78091085A>G GRCh37
NC_000011.8:g.77768733A>G NCBI36
NG_016171.1:g.42784T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000361507.5:c.75+37607T>C MANE Select ENSP00000354952.4:n.75+37607T>C
ENST00000361507.4:c.75+37607T>C ENSP00000354952.4:n.75+37607T>C
ENST00000526030.1:n.177+37607T>C
ENST00000528886.5:c.-40+38198T>C ENSP00000433762.1:n.-40+38198T>C
ENST00000530915.1:c.-127-15936T>C ENSP00000431868.1:n.-127-15936T>C
ENST00000534823.1:n.126+37607T>C
NM_080491.2:c.75+37607T>C NP_536739.1:n.75+37607T>C
XM_006718753.1:c.-127-15936T>C XP_006718816.1:n.-127-15936T>C
XM_006718753.2:c.-127-15936T>C XP_006718816.1:n.-127-15936T>C
NM_080491.3:c.75+37607T>C MANE Select NP_536739.1:n.75+37607T>C