Canonical Allele Identifier: CA447609951

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161530935A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162103929A>G , CM000667.2:g.162103929A>G	GRCh38
NC_000005.9:g.161530935A>G , CM000667.1:g.161530935A>G	GRCh37
NC_000005.8:g.161463513A>G	NCBI36
NG_009290.1:g.41288A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.634A>G
ENST00000361925.9:c.792A>G	ENSP00000354651.5:p.Arg264=
ENST00000522053.2:n.563A>G
ENST00000523372.2:c.755A>G
ENST00000638552.1:c.387A>G	ENSP00000491763.1:p.Arg129=
ENST00000638660.1:c.387A>G	ENSP00000492869.1:p.Arg129=
ENST00000638772.1:c.672A>G	ENSP00000491557.1:p.Arg224=
ENST00000638782.1:n.734A>G
ENST00000638877.1:c.549A>G
ENST00000639046.1:c.63A>G	ENSP00000492659.1:p.Arg21=
ENST00000639111.2:c.672A>G	ENSP00000492125.2:p.Arg224=
ENST00000639213.2:c.672A>G MANE Select	ENSP00000491909.2:p.Arg224=
ENST00000639278.1:c.600A>G	ENSP00000491958.1:p.Arg200=
ENST00000639384.1:c.672A>G	ENSP00000491240.1:p.Arg224=
ENST00000639424.1:c.107+35823A>G	ENSP00000491245.1:n.107+35823A>G
ENST00000639683.1:c.606A>G	ENSP00000492581.1:p.Arg202=
ENST00000639975.1:c.606A>G	ENSP00000492096.1:p.Arg202=
ENST00000640574.1:c.387A>G	ENSP00000491582.1:p.Arg129=
ENST00000640739.1:n.3203A>G
ENST00000640910.1:c.110A>G
ENST00000640985.1:c.585A>G	ENSP00000492293.1:p.Arg195=
ENST00000641017.1:c.672A>G	ENSP00000493461.1:p.Arg224=
ENST00000356592.7:c.672A>G	ENSP00000349000.3:p.Arg224=
ENST00000361925.8:c.672A>G	ENSP00000354651.4:p.Arg224=
ENST00000414552.6:c.792A>G	ENSP00000410732.2:p.Arg264=
ENST00000522053.1:c.387A>G	ENSP00000430182.1:p.Arg129=
ENST00000522990.5:c.*274A>G	ENSP00000430732.1:n.*274A>G
ENST00000523372.1:c.793A>G	ENSP00000430124.1:n.793A>G
NM_000816.3:c.672A>G	NP_000807.2:p.Arg224=
NM_198903.2:c.792A>G	NP_944493.2:p.Arg264=
NM_198904.2:c.672A>G	NP_944494.1:p.Arg224=
NM_001375339.1:c.663A>G	NP_001362268.1:p.Arg221=
NM_001375340.1:c.672A>G	NP_001362269.1:p.Arg224=
NM_001375341.1:c.672A>G	NP_001362270.1:p.Arg224=
NM_001375342.1:c.672A>G	NP_001362271.1:p.Arg224=
NM_001375343.1:c.792A>G	NP_001362272.1:p.Arg264=
NM_001375344.1:c.672A>G	NP_001362273.1:p.Arg224=
NM_001375345.1:c.606A>G	NP_001362274.1:p.Arg202=
NM_001375346.1:c.606A>G	NP_001362275.1:p.Arg202=
NM_001375347.1:c.585A>G	NP_001362276.1:p.Arg195=
NM_001375348.1:c.252A>G	NP_001362277.1:p.Arg84=
NM_001375349.1:c.387A>G	NP_001362278.1:p.Arg129=
NM_001375350.1:c.252A>G	NP_001362279.1:p.Arg84=
NM_198904.3:c.672A>G	NP_944494.1:p.Arg224=
NM_198904.4:c.672A>G MANE Select	NP_944494.1:p.Arg224=