Canonical Allele Identifier: CA13465053
Gene: GAB2 HGNC NCBI

Linked Data

dbSNP Id: rs2373115

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78380104C>A , CM000673.2:g.78380104C>A GRCh38
NC_000011.9:g.78091150C>A , CM000673.1:g.78091150C>A GRCh37
NC_000011.8:g.77768798C>A NCBI36
NG_016171.1:g.42719G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361507.5:c.75+37542G>T MANE Select ENSP00000354952.4:p.=
ENST00000361507.4:c.75+37542G>T ENSP00000354952.4:p.=
ENST00000526030.1:n.177+37542G>T
ENST00000528886.5:c.-40+38133G>T ENSP00000433762.1:p.=
ENST00000530915.1:c.-127-16001G>T ENSP00000431868.1:p.=
ENST00000534823.1:n.126+37542G>T
NM_080491.2:c.75+37542G>T NP_536739.1:p.=
XM_006718753.1:c.-127-16001G>T XP_006718816.1:p.=
XM_006718753.2:c.-127-16001G>T XP_006718816.1:p.=
NM_080491.3:c.75+37542G>T MANE Select NP_536739.1:p.=