Canonical Allele Identifier: CA1596380226
Gene: GABRG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162149109T= , CM000667.2:g.162149109T= GRCh38
NC_000005.9:g.161576115T= , CM000667.1:g.161576115T= GRCh37
NC_000005.8:g.161508693T= NCBI36
NG_009290.1:g.86468T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.925T=
ENST00000361925.9:c.1044T= ENSP00000354651.5:p.Gly348=
ENST00000522053.2:n.815T=
ENST00000523372.2:c.1007T=
ENST00000638253.1:n.178T=
ENST00000638552.1:c.639T= ENSP00000491763.1:p.Gly213=
ENST00000638660.1:c.639T= ENSP00000492869.1:p.Gly213=
ENST00000638772.1:c.924T= ENSP00000491557.1:p.Gly308=
ENST00000638877.1:c.801T=
ENST00000639046.1:c.315T= ENSP00000492659.1:p.Gly105=
ENST00000639111.2:c.924T= ENSP00000492125.2:p.Gly308=
ENST00000639213.2:c.924T= MANE Select ENSP00000491909.2:p.Gly308=
ENST00000639278.1:c.852T= ENSP00000491958.1:p.Gly284=
ENST00000639384.1:c.924T= ENSP00000491240.1:p.Gly308=
ENST00000639424.1:c.*124T= ENSP00000491245.1:n.*124T=
ENST00000639683.1:c.858T= ENSP00000492581.1:p.Gly286=
ENST00000639975.1:c.858T= ENSP00000492096.1:p.Gly286=
ENST00000640500.1:n.222T=
ENST00000640574.1:c.639T= ENSP00000491582.1:p.Gly213=
ENST00000640739.1:n.3455T=
ENST00000640910.1:c.362T=
ENST00000640985.1:c.837T= ENSP00000492293.1:p.Gly279=
ENST00000641017.1:c.924T= ENSP00000493461.1:p.Gly308=
ENST00000356592.7:c.924T= ENSP00000349000.3:p.Gly308=
ENST00000361925.8:c.924T= ENSP00000354651.4:p.Gly308=
ENST00000414552.6:c.1044T= ENSP00000410732.2:p.Gly348=
ENST00000522053.1:c.639T= ENSP00000430182.1:p.Gly213=
ENST00000522990.5:c.*526T= ENSP00000430732.1:n.*526T=
ENST00000523372.1:c.1045T= ENSP00000430124.1:n.1045T=
NM_000816.3:c.924T= NP_000807.2:p.Gly308=
NM_198903.2:c.1044T= NP_944493.2:p.Gly348=
NM_198904.2:c.924T= NP_944494.1:p.Gly308=
NM_001375339.1:c.915T= NP_001362268.1:p.Gly305=
NM_001375340.1:c.923-2621T= NP_001362269.1:n.923-2621T=
NM_001375341.1:c.921T= NP_001362270.1:p.Gly307=
NM_001375342.1:c.921T= NP_001362271.1:p.Gly307=
NM_001375343.1:c.1044T= NP_001362272.1:p.Gly348=
NM_001375344.1:c.963T= NP_001362273.1:p.Gly321=
NM_001375345.1:c.858T= NP_001362274.1:p.Gly286=
NM_001375346.1:c.858T= NP_001362275.1:p.Gly286=
NM_001375347.1:c.837T= NP_001362276.1:p.Gly279=
NM_001375348.1:c.504T= NP_001362277.1:p.Gly168=
NM_001375349.1:c.639T= NP_001362278.1:p.Gly213=
NM_001375350.1:c.504T= NP_001362279.1:p.Gly168=
NM_198904.3:c.924T= NP_944494.1:p.Gly308=
NM_198904.4:c.924T= MANE Select NP_944494.1:p.Gly308=