Canonical Allele Identifier: CA1596380247
Gene: GABRG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162149160G= , CM000667.2:g.162149160G= GRCh38
NC_000005.9:g.161576166G= , CM000667.1:g.161576166G= GRCh37
NC_000005.8:g.161508744G= NCBI36
NG_009290.1:g.86519G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.976G=
ENST00000361925.9:c.1095G= ENSP00000354651.5:p.Ser365=
ENST00000522053.2:n.866G=
ENST00000523372.2:c.1058G=
ENST00000638253.1:n.229G=
ENST00000638552.1:c.690G= ENSP00000491763.1:p.Ser230=
ENST00000638660.1:c.690G= ENSP00000492869.1:p.Ser230=
ENST00000638772.1:c.975G= ENSP00000491557.1:p.Ser325=
ENST00000638877.1:c.852G=
ENST00000639046.1:c.366G= ENSP00000492659.1:p.Ser122=
ENST00000639111.2:c.975G= ENSP00000492125.2:p.Ser325=
ENST00000639213.2:c.975G= MANE Select ENSP00000491909.2:p.Ser325=
ENST00000639278.1:c.903G= ENSP00000491958.1:p.Ser301=
ENST00000639384.1:c.975G= ENSP00000491240.1:p.Ser325=
ENST00000639424.1:c.*175G= ENSP00000491245.1:n.*175G=
ENST00000639683.1:c.909G= ENSP00000492581.1:p.Ser303=
ENST00000639975.1:c.909G= ENSP00000492096.1:p.Ser303=
ENST00000640500.1:n.273G=
ENST00000640574.1:c.690G= ENSP00000491582.1:p.Ser230=
ENST00000640739.1:n.3506G=
ENST00000640910.1:c.413G=
ENST00000640985.1:c.888G= ENSP00000492293.1:p.Ser296=
ENST00000641017.1:c.975G= ENSP00000493461.1:p.Ser325=
ENST00000356592.7:c.975G= ENSP00000349000.3:p.Ser325=
ENST00000361925.8:c.975G= ENSP00000354651.4:p.Ser325=
ENST00000414552.6:c.1095G= ENSP00000410732.2:p.Ser365=
ENST00000522990.5:c.*577G= ENSP00000430732.1:n.*577G=
ENST00000523372.1:c.1096G= ENSP00000430124.1:n.1096G=
NM_000816.3:c.975G= NP_000807.2:p.Ser325=
NM_198903.2:c.1095G= NP_944493.2:p.Ser365=
NM_198904.2:c.975G= NP_944494.1:p.Ser325=
NM_001375339.1:c.966G= NP_001362268.1:p.Ser322=
NM_001375340.1:c.923-2570G= NP_001362269.1:n.923-2570G=
NM_001375341.1:c.972G= NP_001362270.1:p.Ser324=
NM_001375342.1:c.972G= NP_001362271.1:p.Ser324=
NM_001375343.1:c.1095G= NP_001362272.1:p.Ser365=
NM_001375344.1:c.1014G= NP_001362273.1:p.Ser338=
NM_001375345.1:c.909G= NP_001362274.1:p.Ser303=
NM_001375346.1:c.909G= NP_001362275.1:p.Ser303=
NM_001375347.1:c.888G= NP_001362276.1:p.Ser296=
NM_001375348.1:c.555G= NP_001362277.1:p.Ser185=
NM_001375349.1:c.690G= NP_001362278.1:p.Ser230=
NM_001375350.1:c.555G= NP_001362279.1:p.Ser185=
NM_198904.3:c.975G= NP_944494.1:p.Ser325=
NM_198904.4:c.975G= MANE Select NP_944494.1:p.Ser325=