Canonical Allele Identifier: CA1596380246
Gene: GABRG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162149159C= , CM000667.2:g.162149159C= GRCh38
NC_000005.9:g.161576165C= , CM000667.1:g.161576165C= GRCh37
NC_000005.8:g.161508743C= NCBI36
NG_009290.1:g.86518C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.975C=
ENST00000361925.9:c.1094C= ENSP00000354651.5:p.Ser365=
ENST00000522053.2:n.865C=
ENST00000523372.2:c.1057C=
ENST00000638253.1:n.228C=
ENST00000638552.1:c.689C= ENSP00000491763.1:p.Ser230=
ENST00000638660.1:c.689C= ENSP00000492869.1:p.Ser230=
ENST00000638772.1:c.974C= ENSP00000491557.1:p.Ser325=
ENST00000638877.1:c.851C=
ENST00000639046.1:c.365C= ENSP00000492659.1:p.Ser122=
ENST00000639111.2:c.974C= ENSP00000492125.2:p.Ser325=
ENST00000639213.2:c.974C= MANE Select ENSP00000491909.2:p.Ser325=
ENST00000639278.1:c.902C= ENSP00000491958.1:p.Ser301=
ENST00000639384.1:c.974C= ENSP00000491240.1:p.Ser325=
ENST00000639424.1:c.*174C= ENSP00000491245.1:n.*174C=
ENST00000639683.1:c.908C= ENSP00000492581.1:p.Ser303=
ENST00000639975.1:c.908C= ENSP00000492096.1:p.Ser303=
ENST00000640500.1:n.272C=
ENST00000640574.1:c.689C= ENSP00000491582.1:p.Ser230=
ENST00000640739.1:n.3505C=
ENST00000640910.1:c.412C=
ENST00000640985.1:c.887C= ENSP00000492293.1:p.Ser296=
ENST00000641017.1:c.974C= ENSP00000493461.1:p.Ser325=
ENST00000356592.7:c.974C= ENSP00000349000.3:p.Ser325=
ENST00000361925.8:c.974C= ENSP00000354651.4:p.Ser325=
ENST00000414552.6:c.1094C= ENSP00000410732.2:p.Ser365=
ENST00000522990.5:c.*576C= ENSP00000430732.1:n.*576C=
ENST00000523372.1:c.1095C= ENSP00000430124.1:n.1095C=
NM_000816.3:c.974C= NP_000807.2:p.Ser325=
NM_198903.2:c.1094C= NP_944493.2:p.Ser365=
NM_198904.2:c.974C= NP_944494.1:p.Ser325=
NM_001375339.1:c.965C= NP_001362268.1:p.Ser322=
NM_001375340.1:c.923-2571C= NP_001362269.1:n.923-2571C=
NM_001375341.1:c.971C= NP_001362270.1:p.Ser324=
NM_001375342.1:c.971C= NP_001362271.1:p.Ser324=
NM_001375343.1:c.1094C= NP_001362272.1:p.Ser365=
NM_001375344.1:c.1013C= NP_001362273.1:p.Ser338=
NM_001375345.1:c.908C= NP_001362274.1:p.Ser303=
NM_001375346.1:c.908C= NP_001362275.1:p.Ser303=
NM_001375347.1:c.887C= NP_001362276.1:p.Ser296=
NM_001375348.1:c.554C= NP_001362277.1:p.Ser185=
NM_001375349.1:c.689C= NP_001362278.1:p.Ser230=
NM_001375350.1:c.554C= NP_001362279.1:p.Ser185=
NM_198904.3:c.974C= NP_944494.1:p.Ser325=
NM_198904.4:c.974C= MANE Select NP_944494.1:p.Ser325=