Canonical Allele Identifier: CA1596382087
Gene: GABRG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162153211G= , CM000667.2:g.162153211G= GRCh38
NC_000005.9:g.161580217G= , CM000667.1:g.161580217G= GRCh37
NC_000005.8:g.161512795G= NCBI36
NG_009290.1:g.90570G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.1272G=
ENST00000361925.9:c.1367G= ENSP00000354651.5:p.Ser456=
ENST00000523372.2:c.1330G=
ENST00000638253.1:n.525G=
ENST00000638552.1:c.962G= ENSP00000491763.1:p.Ser321=
ENST00000638660.1:c.986G= ENSP00000492869.1:p.Ser329=
ENST00000638772.1:c.*3868G= ENSP00000491557.1:n.*3868G=
ENST00000638877.1:c.1148G=
ENST00000639046.1:c.638G= ENSP00000492659.1:p.Ser213=
ENST00000639111.2:c.1247G= ENSP00000492125.2:p.Ser416=
ENST00000639213.2:c.1271G= MANE Select ENSP00000491909.2:p.Ser424=
ENST00000639278.1:c.1934G= ENSP00000491958.1:n.1934G=
ENST00000639384.1:c.*1452G= ENSP00000491240.1:n.*1452G=
ENST00000639424.1:c.*471G= ENSP00000491245.1:n.*471G=
ENST00000639683.1:c.1205G= ENSP00000492581.1:p.Ser402=
ENST00000639975.1:c.1181G= ENSP00000492096.1:p.Ser394=
ENST00000640500.1:n.545G=
ENST00000640739.1:n.6218G=
ENST00000640910.1:c.709G=
ENST00000640985.1:c.1184G= ENSP00000492293.1:p.Ser395=
ENST00000641017.1:c.1340G= ENSP00000493461.1:p.Ser447=
ENST00000356592.7:c.1271G= ENSP00000349000.3:p.Ser424=
ENST00000361925.8:c.1247G= ENSP00000354651.4:p.Ser416=
ENST00000414552.6:c.1391G= ENSP00000410732.2:p.Ser464=
ENST00000522990.5:c.*849G= ENSP00000430732.1:n.*849G=
ENST00000523372.1:c.1368G= ENSP00000430124.1:n.1368G=
NM_000816.3:c.1247G= NP_000807.2:p.Ser416=
NM_198903.2:c.1391G= NP_944493.2:p.Ser464=
NM_198904.2:c.1271G= NP_944494.1:p.Ser424=
NM_001375339.1:c.1262G= NP_001362268.1:p.Ser421=
NM_001375340.1:c.*105G= NP_001362269.1:n.*105G=
NM_001375341.1:c.1268G= NP_001362270.1:p.Ser423=
NM_001375342.1:c.1244G= NP_001362271.1:p.Ser415=
NM_001375343.1:c.1367G= NP_001362272.1:p.Ser456=
NM_001375344.1:c.1310G= NP_001362273.1:p.Ser437=
NM_001375345.1:c.1181G= NP_001362274.1:p.Ser394=
NM_001375346.1:c.1205G= NP_001362275.1:p.Ser402=
NM_001375347.1:c.1184G= NP_001362276.1:p.Ser395=
NM_001375348.1:c.827G= NP_001362277.1:p.Ser276=
NM_001375349.1:c.962G= NP_001362278.1:p.Ser321=
NM_001375350.1:c.851G= NP_001362279.1:p.Ser284=
NM_198904.3:c.1271G= NP_944494.1:p.Ser424=
NM_198904.4:c.1271G= MANE Select NP_944494.1:p.Ser424=