Canonical Allele Identifier: CA447609927

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161530908T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162103902T>A , CM000667.2:g.162103902T>A	GRCh38
NC_000005.9:g.161530908T>A , CM000667.1:g.161530908T>A	GRCh37
NC_000005.8:g.161463486T>A	NCBI36
NG_009290.1:g.41261T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000356592.8:c.607T>A
ENST00000361925.9:c.765T>A	ENSP00000354651.5:p.Arg255=
ENST00000522053.2:n.536T>A
ENST00000523372.2:c.728T>A
ENST00000638552.1:c.360T>A	ENSP00000491763.1:p.Arg120=
ENST00000638660.1:c.360T>A	ENSP00000492869.1:p.Arg120=
ENST00000638772.1:c.645T>A	ENSP00000491557.1:p.Arg215=
ENST00000638782.1:n.707T>A
ENST00000638877.1:c.522T>A
ENST00000639046.1:c.36T>A	ENSP00000492659.1:p.Arg12=
ENST00000639111.2:c.645T>A	ENSP00000492125.2:p.Arg215=
ENST00000639213.2:c.645T>A MANE Select	ENSP00000491909.2:p.Arg215=
ENST00000639278.1:c.573T>A	ENSP00000491958.1:p.Arg191=
ENST00000639384.1:c.645T>A	ENSP00000491240.1:p.Arg215=
ENST00000639424.1:c.107+35796T>A	ENSP00000491245.1:n.107+35796T>A
ENST00000639683.1:c.579T>A	ENSP00000492581.1:p.Arg193=
ENST00000639975.1:c.579T>A	ENSP00000492096.1:p.Arg193=
ENST00000640574.1:c.360T>A	ENSP00000491582.1:p.Arg120=
ENST00000640739.1:n.3176T>A
ENST00000640910.1:c.83T>A
ENST00000640985.1:c.558T>A	ENSP00000492293.1:p.Arg186=
ENST00000641017.1:c.645T>A	ENSP00000493461.1:p.Arg215=
ENST00000356592.7:c.645T>A	ENSP00000349000.3:p.Arg215=
ENST00000361925.8:c.645T>A	ENSP00000354651.4:p.Arg215=
ENST00000414552.6:c.765T>A	ENSP00000410732.2:p.Arg255=
ENST00000522053.1:c.360T>A	ENSP00000430182.1:p.Arg120=
ENST00000522990.5:c.*247T>A	ENSP00000430732.1:n.*247T>A
ENST00000523372.1:c.766T>A	ENSP00000430124.1:n.766T>A
NM_000816.3:c.645T>A	NP_000807.2:p.Arg215=
NM_198903.2:c.765T>A	NP_944493.2:p.Arg255=
NM_198904.2:c.645T>A	NP_944494.1:p.Arg215=
NM_001375339.1:c.636T>A	NP_001362268.1:p.Arg212=
NM_001375340.1:c.645T>A	NP_001362269.1:p.Arg215=
NM_001375341.1:c.645T>A	NP_001362270.1:p.Arg215=
NM_001375342.1:c.645T>A	NP_001362271.1:p.Arg215=
NM_001375343.1:c.765T>A	NP_001362272.1:p.Arg255=
NM_001375344.1:c.645T>A	NP_001362273.1:p.Arg215=
NM_001375345.1:c.579T>A	NP_001362274.1:p.Arg193=
NM_001375346.1:c.579T>A	NP_001362275.1:p.Arg193=
NM_001375347.1:c.558T>A	NP_001362276.1:p.Arg186=
NM_001375348.1:c.225T>A	NP_001362277.1:p.Arg75=
NM_001375349.1:c.360T>A	NP_001362278.1:p.Arg120=
NM_001375350.1:c.225T>A	NP_001362279.1:p.Arg75=
NM_198904.3:c.645T>A	NP_944494.1:p.Arg215=
NM_198904.4:c.645T>A MANE Select	NP_944494.1:p.Arg215=