Canonical Allele Identifier: CA1596365204
Gene: GABRG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162103909A= , CM000667.2:g.162103909A= GRCh38
NC_000005.9:g.161530915A= , CM000667.1:g.161530915A= GRCh37
NC_000005.8:g.161463493A= NCBI36
NG_009290.1:g.41268A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.614A=
ENST00000361925.9:c.772A= ENSP00000354651.5:p.Ile258=
ENST00000522053.2:n.543A=
ENST00000523372.2:c.735A=
ENST00000638552.1:c.367A= ENSP00000491763.1:p.Ile123=
ENST00000638660.1:c.367A= ENSP00000492869.1:p.Ile123=
ENST00000638772.1:c.652A= ENSP00000491557.1:p.Ile218=
ENST00000638782.1:n.714A=
ENST00000638877.1:c.529A=
ENST00000639046.1:c.43A= ENSP00000492659.1:p.Ile15=
ENST00000639111.2:c.652A= ENSP00000492125.2:p.Ile218=
ENST00000639213.2:c.652A= MANE Select ENSP00000491909.2:p.Ile218=
ENST00000639278.1:c.580A= ENSP00000491958.1:p.Ile194=
ENST00000639384.1:c.652A= ENSP00000491240.1:p.Ile218=
ENST00000639424.1:c.107+35803A= ENSP00000491245.1:n.107+35803A=
ENST00000639683.1:c.586A= ENSP00000492581.1:p.Ile196=
ENST00000639975.1:c.586A= ENSP00000492096.1:p.Ile196=
ENST00000640574.1:c.367A= ENSP00000491582.1:p.Ile123=
ENST00000640739.1:n.3183A=
ENST00000640910.1:c.90A=
ENST00000640985.1:c.565A= ENSP00000492293.1:p.Ile189=
ENST00000641017.1:c.652A= ENSP00000493461.1:p.Ile218=
ENST00000356592.7:c.652A= ENSP00000349000.3:p.Ile218=
ENST00000361925.8:c.652A= ENSP00000354651.4:p.Ile218=
ENST00000414552.6:c.772A= ENSP00000410732.2:p.Ile258=
ENST00000522053.1:c.367A= ENSP00000430182.1:p.Ile123=
ENST00000522990.5:c.*254A= ENSP00000430732.1:n.*254A=
ENST00000523372.1:c.773A= ENSP00000430124.1:n.773A=
NM_000816.3:c.652A= NP_000807.2:p.Ile218=
NM_198903.2:c.772A= NP_944493.2:p.Ile258=
NM_198904.2:c.652A= NP_944494.1:p.Ile218=
NM_001375339.1:c.643A= NP_001362268.1:p.Ile215=
NM_001375340.1:c.652A= NP_001362269.1:p.Ile218=
NM_001375341.1:c.652A= NP_001362270.1:p.Ile218=
NM_001375342.1:c.652A= NP_001362271.1:p.Ile218=
NM_001375343.1:c.772A= NP_001362272.1:p.Ile258=
NM_001375344.1:c.652A= NP_001362273.1:p.Ile218=
NM_001375345.1:c.586A= NP_001362274.1:p.Ile196=
NM_001375346.1:c.586A= NP_001362275.1:p.Ile196=
NM_001375347.1:c.565A= NP_001362276.1:p.Ile189=
NM_001375348.1:c.232A= NP_001362277.1:p.Ile78=
NM_001375349.1:c.367A= NP_001362278.1:p.Ile123=
NM_001375350.1:c.232A= NP_001362279.1:p.Ile78=
NM_198904.3:c.652A= NP_944494.1:p.Ile218=
NM_198904.4:c.652A= MANE Select NP_944494.1:p.Ile218=