Canonical Allele Identifier: CA1596380275
Gene: GABRG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162149255A= , CM000667.2:g.162149255A= GRCh38
NC_000005.9:g.161576261A= , CM000667.1:g.161576261A= GRCh37
NC_000005.8:g.161508839A= NCBI36
NG_009290.1:g.86614A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.1071A=
ENST00000361925.9:c.1190A= ENSP00000354651.5:p.His397=
ENST00000523372.2:c.1153A=
ENST00000638253.1:n.324A=
ENST00000638552.1:c.785A= ENSP00000491763.1:p.His262=
ENST00000638660.1:c.785A= ENSP00000492869.1:p.His262=
ENST00000638772.1:c.1070A= ENSP00000491557.1:p.His357=
ENST00000638877.1:c.947A=
ENST00000639046.1:c.461A= ENSP00000492659.1:p.His154=
ENST00000639111.2:c.1070A= ENSP00000492125.2:p.His357=
ENST00000639213.2:c.1070A= MANE Select ENSP00000491909.2:p.His357=
ENST00000639278.1:c.998A= ENSP00000491958.1:p.His333=
ENST00000639384.1:c.1070A= ENSP00000491240.1:p.His357=
ENST00000639424.1:c.*270A= ENSP00000491245.1:n.*270A=
ENST00000639683.1:c.1004A= ENSP00000492581.1:p.His335=
ENST00000639975.1:c.1004A= ENSP00000492096.1:p.His335=
ENST00000640500.1:n.368A=
ENST00000640574.1:c.785A= ENSP00000491582.1:p.His262=
ENST00000640739.1:n.3601A=
ENST00000640910.1:c.508A=
ENST00000640985.1:c.983A= ENSP00000492293.1:p.His328=
ENST00000641017.1:c.1070A= ENSP00000493461.1:p.His357=
ENST00000356592.7:c.1070A= ENSP00000349000.3:p.His357=
ENST00000361925.8:c.1070A= ENSP00000354651.4:p.His357=
ENST00000414552.6:c.1190A= ENSP00000410732.2:p.His397=
ENST00000522990.5:c.*672A= ENSP00000430732.1:n.*672A=
ENST00000523372.1:c.1191A= ENSP00000430124.1:n.1191A=
NM_000816.3:c.1070A= NP_000807.2:p.His357=
NM_198903.2:c.1190A= NP_944493.2:p.His397=
NM_198904.2:c.1070A= NP_944494.1:p.His357=
NM_001375339.1:c.1061A= NP_001362268.1:p.His354=
NM_001375340.1:c.923-2475A= NP_001362269.1:n.923-2475A=
NM_001375341.1:c.1067A= NP_001362270.1:p.His356=
NM_001375342.1:c.1067A= NP_001362271.1:p.His356=
NM_001375343.1:c.1190A= NP_001362272.1:p.His397=
NM_001375344.1:c.1109A= NP_001362273.1:p.His370=
NM_001375345.1:c.1004A= NP_001362274.1:p.His335=
NM_001375346.1:c.1004A= NP_001362275.1:p.His335=
NM_001375347.1:c.983A= NP_001362276.1:p.His328=
NM_001375348.1:c.650A= NP_001362277.1:p.His217=
NM_001375349.1:c.785A= NP_001362278.1:p.His262=
NM_001375350.1:c.650A= NP_001362279.1:p.His217=
NM_198904.3:c.1070A= NP_944494.1:p.His357=
NM_198904.4:c.1070A= MANE Select NP_944494.1:p.His357=