Canonical Allele Identifier: CA16013817
Gene: GAB3 HGNC NCBI

Linked Data

dbSNP Id: rs2664170

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154717327G>A , CM000685.2:g.154717327G>A GRCh38
NC_000023.10:g.153945602G>A , CM000685.1:g.153945602G>A GRCh37
NC_000023.9:g.153598796G>A NCBI36
NG_012834.2:g.38747C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369568.8:c.73-998C>T ENSP00000358581.4:p.=
ENST00000369575.7:c.73-998C>T ENSP00000358588.3:p.=
ENST00000424127.2:c.73-998C>T ENSP00000399588.2:p.=
NM_001081573.2:c.73-998C>T NP_001075042.1:p.=
NM_001282283.1:c.73-998C>T NP_001269212.1:p.=
NM_080612.3:c.73-998C>T NP_542179.1:p.=
XM_005274648.1:c.73-998C>T XP_005274705.1:p.=
XM_006724804.1:c.73-998C>T XP_006724867.1:p.=
XM_006724806.2:c.73-998C>T XP_006724869.1:p.=
XM_011531103.1:c.73-998C>T XP_011529405.1:p.=
XM_011531104.1:c.73-998C>T XP_011529406.1:p.=
XM_011531105.1:c.73-998C>T XP_011529407.1:p.=
XM_011531106.1:c.73-998C>T XP_011529408.1:p.=
XM_017029276.1:c.73-998C>T XP_016884765.1:p.=
NM_001081573.3:c.73-998C>T MANE Select NP_001075042.1:p.=
NM_001282283.2:c.73-998C>T NP_001269212.1:p.=
NM_080612.4:c.73-998C>T NP_542179.1:p.=