Canonical Allele Identifier: CA1596365223
Gene: GABRG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162103962G= , CM000667.2:g.162103962G= GRCh38
NC_000005.9:g.161530968G= , CM000667.1:g.161530968G= GRCh37
NC_000005.8:g.161463546G= NCBI36
NG_009290.1:g.41321G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.667G=
ENST00000361925.9:c.825G= ENSP00000354651.5:p.Trp275=
ENST00000522053.2:n.596G=
ENST00000523372.2:c.788G=
ENST00000638552.1:c.420G= ENSP00000491763.1:p.Trp140=
ENST00000638660.1:c.420G= ENSP00000492869.1:p.Trp140=
ENST00000638772.1:c.705G= ENSP00000491557.1:p.Trp235=
ENST00000638782.1:n.767G=
ENST00000638877.1:c.582G=
ENST00000639046.1:c.96G= ENSP00000492659.1:p.Trp32=
ENST00000639111.2:c.705G= ENSP00000492125.2:p.Trp235=
ENST00000639213.2:c.705G= MANE Select ENSP00000491909.2:p.Trp235=
ENST00000639278.1:c.633G= ENSP00000491958.1:p.Trp211=
ENST00000639384.1:c.705G= ENSP00000491240.1:p.Trp235=
ENST00000639424.1:c.107+35856G= ENSP00000491245.1:n.107+35856G=
ENST00000639683.1:c.639G= ENSP00000492581.1:p.Trp213=
ENST00000639975.1:c.639G= ENSP00000492096.1:p.Trp213=
ENST00000640574.1:c.420G= ENSP00000491582.1:p.Trp140=
ENST00000640739.1:n.3236G=
ENST00000640910.1:c.143G=
ENST00000640985.1:c.618G= ENSP00000492293.1:p.Trp206=
ENST00000641017.1:c.705G= ENSP00000493461.1:p.Trp235=
ENST00000356592.7:c.705G= ENSP00000349000.3:p.Trp235=
ENST00000361925.8:c.705G= ENSP00000354651.4:p.Trp235=
ENST00000414552.6:c.825G= ENSP00000410732.2:p.Trp275=
ENST00000522053.1:c.420G= ENSP00000430182.1:p.Trp140=
ENST00000522990.5:c.*307G= ENSP00000430732.1:n.*307G=
ENST00000523372.1:c.826G= ENSP00000430124.1:n.826G=
NM_000816.3:c.705G= NP_000807.2:p.Trp235=
NM_198903.2:c.825G= NP_944493.2:p.Trp275=
NM_198904.2:c.705G= NP_944494.1:p.Trp235=
NM_001375339.1:c.696G= NP_001362268.1:p.Trp232=
NM_001375340.1:c.705G= NP_001362269.1:p.Trp235=
NM_001375341.1:c.705G= NP_001362270.1:p.Trp235=
NM_001375342.1:c.705G= NP_001362271.1:p.Trp235=
NM_001375343.1:c.825G= NP_001362272.1:p.Trp275=
NM_001375344.1:c.705G= NP_001362273.1:p.Trp235=
NM_001375345.1:c.639G= NP_001362274.1:p.Trp213=
NM_001375346.1:c.639G= NP_001362275.1:p.Trp213=
NM_001375347.1:c.618G= NP_001362276.1:p.Trp206=
NM_001375348.1:c.285G= NP_001362277.1:p.Trp95=
NM_001375349.1:c.420G= NP_001362278.1:p.Trp140=
NM_001375350.1:c.285G= NP_001362279.1:p.Trp95=
NM_198904.3:c.705G= NP_944494.1:p.Trp235=
NM_198904.4:c.705G= MANE Select NP_944494.1:p.Trp235=