Canonical Allele Identifier: CA447691836

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161580243C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153237C>A , CM000667.2:g.162153237C>A	GRCh38
NC_000005.9:g.161580243C>A , CM000667.1:g.161580243C>A	GRCh37
NC_000005.8:g.161512821C>A	NCBI36
NG_009290.1:g.90596C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1298C>A
ENST00000361925.9:c.1393C>A	ENSP00000354651.5:p.Arg465=
ENST00000523372.2:c.1356C>A
ENST00000638253.1:n.551C>A
ENST00000638552.1:c.988C>A	ENSP00000491763.1:p.Arg330=
ENST00000638660.1:c.1012C>A	ENSP00000492869.1:p.Arg338=
ENST00000638772.1:c.*3894C>A	ENSP00000491557.1:n.*3894C>A
ENST00000638877.1:c.1174C>A
ENST00000639046.1:c.664C>A	ENSP00000492659.1:p.Arg222=
ENST00000639111.2:c.1273C>A	ENSP00000492125.2:p.Arg425=
ENST00000639213.2:c.1297C>A MANE Select	ENSP00000491909.2:p.Arg433=
ENST00000639278.1:c.1960C>A	ENSP00000491958.1:n.1960C>A
ENST00000639384.1:c.*1478C>A	ENSP00000491240.1:n.*1478C>A
ENST00000639424.1:c.*497C>A	ENSP00000491245.1:n.*497C>A
ENST00000639683.1:c.1231C>A	ENSP00000492581.1:p.Arg411=
ENST00000639975.1:c.1207C>A	ENSP00000492096.1:p.Arg403=
ENST00000640500.1:n.571C>A
ENST00000640739.1:n.6244C>A
ENST00000640910.1:c.735C>A
ENST00000640985.1:c.1210C>A	ENSP00000492293.1:p.Arg404=
ENST00000641017.1:c.1366C>A	ENSP00000493461.1:p.Arg456=
ENST00000356592.7:c.1297C>A	ENSP00000349000.3:p.Arg433=
ENST00000361925.8:c.1273C>A	ENSP00000354651.4:p.Arg425=
ENST00000414552.6:c.1417C>A	ENSP00000410732.2:p.Arg473=
ENST00000522990.5:c.*875C>A	ENSP00000430732.1:n.*875C>A
ENST00000523372.1:c.1394C>A	ENSP00000430124.1:n.1394C>A
NM_000816.3:c.1273C>A	NP_000807.2:p.Arg425=
NM_198903.2:c.1417C>A	NP_944493.2:p.Arg473=
NM_198904.2:c.1297C>A	NP_944494.1:p.Arg433=
NM_001375339.1:c.1288C>A	NP_001362268.1:p.Arg430=
NM_001375340.1:c.*131C>A	NP_001362269.1:n.*131C>A
NM_001375341.1:c.1294C>A	NP_001362270.1:p.Arg432=
NM_001375342.1:c.1270C>A	NP_001362271.1:p.Arg424=
NM_001375343.1:c.1393C>A	NP_001362272.1:p.Arg465=
NM_001375344.1:c.1336C>A	NP_001362273.1:p.Arg446=
NM_001375345.1:c.1207C>A	NP_001362274.1:p.Arg403=
NM_001375346.1:c.1231C>A	NP_001362275.1:p.Arg411=
NM_001375347.1:c.1210C>A	NP_001362276.1:p.Arg404=
NM_001375348.1:c.853C>A	NP_001362277.1:p.Arg285=
NM_001375349.1:c.988C>A	NP_001362278.1:p.Arg330=
NM_001375350.1:c.877C>A	NP_001362279.1:p.Arg293=
NM_198904.3:c.1297C>A	NP_944494.1:p.Arg433=
NM_198904.4:c.1297C>A MANE Select	NP_944494.1:p.Arg433=