Canonical Allele Identifier: CA1596382225
Gene: GABRG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162153301G= , CM000667.2:g.162153301G= GRCh38
NC_000005.9:g.161580307G= , CM000667.1:g.161580307G= GRCh37
NC_000005.8:g.161512885G= NCBI36
NG_009290.1:g.90660G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.1362G=
ENST00000361925.9:c.1457G= ENSP00000354651.5:p.Arg486=
ENST00000523372.2:c.1420G=
ENST00000638253.1:n.615G=
ENST00000638552.1:c.1052G= ENSP00000491763.1:p.Arg351=
ENST00000638660.1:c.1076G= ENSP00000492869.1:p.Arg359=
ENST00000638772.1:c.*3958G= ENSP00000491557.1:n.*3958G=
ENST00000638877.1:c.1238G=
ENST00000639046.1:c.728G= ENSP00000492659.1:p.Arg243=
ENST00000639111.2:c.1337G= ENSP00000492125.2:p.Arg446=
ENST00000639213.2:c.1361G= MANE Select ENSP00000491909.2:p.Arg454=
ENST00000639278.1:c.2024G= ENSP00000491958.1:n.2024G=
ENST00000639384.1:c.*1542G= ENSP00000491240.1:n.*1542G=
ENST00000639424.1:c.*561G= ENSP00000491245.1:n.*561G=
ENST00000639683.1:c.1295G= ENSP00000492581.1:p.Arg432=
ENST00000639975.1:c.1271G= ENSP00000492096.1:p.Arg424=
ENST00000640500.1:n.635G=
ENST00000640739.1:n.6308G=
ENST00000640910.1:c.799G=
ENST00000640985.1:c.1274G= ENSP00000492293.1:p.Arg425=
ENST00000641017.1:c.1430G= ENSP00000493461.1:p.Arg477=
ENST00000356592.7:c.1361G= ENSP00000349000.3:p.Arg454=
ENST00000361925.8:c.1337G= ENSP00000354651.4:p.Arg446=
ENST00000414552.6:c.1481G= ENSP00000410732.2:p.Arg494=
ENST00000522990.5:c.*939G= ENSP00000430732.1:n.*939G=
ENST00000523372.1:c.1458G= ENSP00000430124.1:n.1458G=
NM_000816.3:c.1337G= NP_000807.2:p.Arg446=
NM_198903.2:c.1481G= NP_944493.2:p.Arg494=
NM_198904.2:c.1361G= NP_944494.1:p.Arg454=
NM_001375339.1:c.1352G= NP_001362268.1:p.Arg451=
NM_001375340.1:c.*195G= NP_001362269.1:n.*195G=
NM_001375341.1:c.1358G= NP_001362270.1:p.Arg453=
NM_001375342.1:c.1334G= NP_001362271.1:p.Arg445=
NM_001375343.1:c.1457G= NP_001362272.1:p.Arg486=
NM_001375344.1:c.1400G= NP_001362273.1:p.Arg467=
NM_001375345.1:c.1271G= NP_001362274.1:p.Arg424=
NM_001375346.1:c.1295G= NP_001362275.1:p.Arg432=
NM_001375347.1:c.1274G= NP_001362276.1:p.Arg425=
NM_001375348.1:c.917G= NP_001362277.1:p.Arg306=
NM_001375349.1:c.1052G= NP_001362278.1:p.Arg351=
NM_001375350.1:c.941G= NP_001362279.1:p.Arg314=
NM_198904.3:c.1361G= NP_944494.1:p.Arg454=
NM_198904.4:c.1361G= MANE Select NP_944494.1:p.Arg454=