Canonical Allele Identifier: CA1596382269
Gene: GABRG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162153339G= , CM000667.2:g.162153339G= GRCh38
NC_000005.9:g.161580345G= , CM000667.1:g.161580345G= GRCh37
NC_000005.8:g.161512923G= NCBI36
NG_009290.1:g.90698G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.1400G=
ENST00000361925.9:c.1495G= ENSP00000354651.5:p.Val499=
ENST00000523372.2:c.1458G=
ENST00000638253.1:n.653G=
ENST00000638552.1:c.1090G= ENSP00000491763.1:p.Val364=
ENST00000638660.1:c.1114G= ENSP00000492869.1:p.Val372=
ENST00000638772.1:c.*3996G= ENSP00000491557.1:n.*3996G=
ENST00000638877.1:c.1276G=
ENST00000639046.1:c.766G= ENSP00000492659.1:p.Val256=
ENST00000639111.2:c.1375G= ENSP00000492125.2:p.Val459=
ENST00000639213.2:c.1399G= MANE Select ENSP00000491909.2:p.Val467=
ENST00000639278.1:c.2062G= ENSP00000491958.1:n.2062G=
ENST00000639384.1:c.*1580G= ENSP00000491240.1:n.*1580G=
ENST00000639424.1:c.*599G= ENSP00000491245.1:n.*599G=
ENST00000639683.1:c.1333G= ENSP00000492581.1:p.Val445=
ENST00000639975.1:c.1309G= ENSP00000492096.1:p.Val437=
ENST00000640500.1:n.673G=
ENST00000640739.1:n.6346G=
ENST00000640910.1:c.837G=
ENST00000640985.1:c.1312G= ENSP00000492293.1:p.Val438=
ENST00000641017.1:c.1468G= ENSP00000493461.1:p.Val490=
ENST00000356592.7:c.1399G= ENSP00000349000.3:p.Val467=
ENST00000361925.8:c.1375G= ENSP00000354651.4:p.Val459=
ENST00000414552.6:c.1519G= ENSP00000410732.2:p.Val507=
ENST00000522990.5:c.*977G= ENSP00000430732.1:n.*977G=
ENST00000523372.1:c.1496G= ENSP00000430124.1:n.1496G=
NM_000816.3:c.1375G= NP_000807.2:p.Val459=
NM_198903.2:c.1519G= NP_944493.2:p.Val507=
NM_198904.2:c.1399G= NP_944494.1:p.Val467=
NM_001375339.1:c.1390G= NP_001362268.1:p.Val464=
NM_001375340.1:c.*233G= NP_001362269.1:n.*233G=
NM_001375341.1:c.1396G= NP_001362270.1:p.Val466=
NM_001375342.1:c.1372G= NP_001362271.1:p.Val458=
NM_001375343.1:c.1495G= NP_001362272.1:p.Val499=
NM_001375344.1:c.1438G= NP_001362273.1:p.Val480=
NM_001375345.1:c.1309G= NP_001362274.1:p.Val437=
NM_001375346.1:c.1333G= NP_001362275.1:p.Val445=
NM_001375347.1:c.1312G= NP_001362276.1:p.Val438=
NM_001375348.1:c.955G= NP_001362277.1:p.Val319=
NM_001375349.1:c.1090G= NP_001362278.1:p.Val364=
NM_001375350.1:c.979G= NP_001362279.1:p.Val327=
NM_198904.3:c.1399G= NP_944494.1:p.Val467=
NM_198904.4:c.1399G= MANE Select NP_944494.1:p.Val467=