Canonical Allele Identifier: CA1596382317
Gene: GABRG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162153367G= , CM000667.2:g.162153367G= GRCh38
NC_000005.9:g.161580373G= , CM000667.1:g.161580373G= GRCh37
NC_000005.8:g.161512951G= NCBI36
NG_009290.1:g.90726G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.1428G=
ENST00000361925.9:c.1523G= ENSP00000354651.5:p.Ter508=
ENST00000523372.2:c.1486G=
ENST00000638253.1:n.681G=
ENST00000638552.1:c.1118G= ENSP00000491763.1:p.Ter373=
ENST00000638660.1:c.1142G= ENSP00000492869.1:p.Ter381=
ENST00000638772.1:c.*4024G= ENSP00000491557.1:n.*4024G=
ENST00000638877.1:c.1304G=
ENST00000639046.1:c.794G= ENSP00000492659.1:p.Ter265=
ENST00000639111.2:c.1403G= ENSP00000492125.2:p.Ter468=
ENST00000639213.2:c.1427G= MANE Select ENSP00000491909.2:p.Ter476=
ENST00000639278.1:c.2090G= ENSP00000491958.1:n.2090G=
ENST00000639384.1:c.*1608G= ENSP00000491240.1:n.*1608G=
ENST00000639424.1:c.*627G= ENSP00000491245.1:n.*627G=
ENST00000639683.1:c.1361G= ENSP00000492581.1:p.Ter454=
ENST00000639975.1:c.1337G= ENSP00000492096.1:p.Ter446=
ENST00000640500.1:n.701G=
ENST00000640739.1:n.6374G=
ENST00000640910.1:c.865G=
ENST00000640985.1:c.1340G= ENSP00000492293.1:p.Ter447=
ENST00000641017.1:c.1496G= ENSP00000493461.1:p.Ter499=
ENST00000356592.7:c.1427G= ENSP00000349000.3:p.Ter476=
ENST00000361925.8:c.1403G= ENSP00000354651.4:p.Ter468=
ENST00000414552.6:c.1547G= ENSP00000410732.2:p.Ter516=
ENST00000522990.5:c.*1005G= ENSP00000430732.1:n.*1005G=
ENST00000523372.1:c.1524G= ENSP00000430124.1:n.1524G=
NM_000816.3:c.1403G= NP_000807.2:p.Ter468=
NM_198903.2:c.1547G= NP_944493.2:p.Ter516=
NM_198904.2:c.1427G= NP_944494.1:p.Ter476=
NM_001375339.1:c.1418G= NP_001362268.1:p.Ter473=
NM_001375340.1:c.*261G= NP_001362269.1:n.*261G=
NM_001375341.1:c.1424G= NP_001362270.1:p.Ter475=
NM_001375342.1:c.1400G= NP_001362271.1:p.Ter467=
NM_001375343.1:c.1523G= NP_001362272.1:p.Ter508=
NM_001375344.1:c.1466G= NP_001362273.1:p.Ter489=
NM_001375345.1:c.1337G= NP_001362274.1:p.Ter446=
NM_001375346.1:c.1361G= NP_001362275.1:p.Ter454=
NM_001375347.1:c.1340G= NP_001362276.1:p.Ter447=
NM_001375348.1:c.983G= NP_001362277.1:p.Ter328=
NM_001375349.1:c.1118G= NP_001362278.1:p.Ter373=
NM_001375350.1:c.1007G= NP_001362279.1:p.Ter336=
NM_198904.3:c.1427G= NP_944494.1:p.Ter476=
NM_198904.4:c.1427G= MANE Select NP_944494.1:p.Ter476=