Canonical Allele Identifier: CA1984668703
Gene: GAB2 HGNC NCBI

Linked Data

dbSNP Id: rs1856678509

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78380082T>A , CM000673.2:g.78380082T>A GRCh38
NC_000011.9:g.78091128T>A , CM000673.1:g.78091128T>A GRCh37
NC_000011.8:g.77768776T>A NCBI36
NG_016171.1:g.42741A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361507.5:c.75+37564A>T MANE Select ENSP00000354952.4:n.75+37564A>T
ENST00000361507.4:c.75+37564A>T ENSP00000354952.4:n.75+37564A>T
ENST00000526030.1:n.177+37564A>T
ENST00000528886.5:c.-40+38155A>T ENSP00000433762.1:n.-40+38155A>T
ENST00000530915.1:c.-127-15979A>T ENSP00000431868.1:n.-127-15979A>T
ENST00000534823.1:n.126+37564A>T
NM_080491.2:c.75+37564A>T NP_536739.1:n.75+37564A>T
XM_006718753.1:c.-127-15979A>T XP_006718816.1:n.-127-15979A>T
XM_006718753.2:c.-127-15979A>T XP_006718816.1:n.-127-15979A>T
NM_080491.3:c.75+37564A>T MANE Select NP_536739.1:n.75+37564A>T