Canonical Allele Identifier: CA447691902

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161580267A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153261A>C , CM000667.2:g.162153261A>C	GRCh38
NC_000005.9:g.161580267A>C , CM000667.1:g.161580267A>C	GRCh37
NC_000005.8:g.161512845A>C	NCBI36
NG_009290.1:g.90620A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1322A>C
ENST00000361925.9:c.1417A>C	ENSP00000354651.5:p.Arg473=
ENST00000523372.2:c.1380A>C
ENST00000638253.1:n.575A>C
ENST00000638552.1:c.1012A>C	ENSP00000491763.1:p.Arg338=
ENST00000638660.1:c.1036A>C	ENSP00000492869.1:p.Arg346=
ENST00000638772.1:c.*3918A>C	ENSP00000491557.1:n.*3918A>C
ENST00000638877.1:c.1198A>C
ENST00000639046.1:c.688A>C	ENSP00000492659.1:p.Arg230=
ENST00000639111.2:c.1297A>C	ENSP00000492125.2:p.Arg433=
ENST00000639213.2:c.1321A>C MANE Select	ENSP00000491909.2:p.Arg441=
ENST00000639278.1:c.1984A>C	ENSP00000491958.1:n.1984A>C
ENST00000639384.1:c.*1502A>C	ENSP00000491240.1:n.*1502A>C
ENST00000639424.1:c.*521A>C	ENSP00000491245.1:n.*521A>C
ENST00000639683.1:c.1255A>C	ENSP00000492581.1:p.Arg419=
ENST00000639975.1:c.1231A>C	ENSP00000492096.1:p.Arg411=
ENST00000640500.1:n.595A>C
ENST00000640739.1:n.6268A>C
ENST00000640910.1:c.759A>C
ENST00000640985.1:c.1234A>C	ENSP00000492293.1:p.Arg412=
ENST00000641017.1:c.1390A>C	ENSP00000493461.1:p.Arg464=
ENST00000356592.7:c.1321A>C	ENSP00000349000.3:p.Arg441=
ENST00000361925.8:c.1297A>C	ENSP00000354651.4:p.Arg433=
ENST00000414552.6:c.1441A>C	ENSP00000410732.2:p.Arg481=
ENST00000522990.5:c.*899A>C	ENSP00000430732.1:n.*899A>C
ENST00000523372.1:c.1418A>C	ENSP00000430124.1:n.1418A>C
NM_000816.3:c.1297A>C	NP_000807.2:p.Arg433=
NM_198903.2:c.1441A>C	NP_944493.2:p.Arg481=
NM_198904.2:c.1321A>C	NP_944494.1:p.Arg441=
NM_001375339.1:c.1312A>C	NP_001362268.1:p.Arg438=
NM_001375340.1:c.*155A>C	NP_001362269.1:n.*155A>C
NM_001375341.1:c.1318A>C	NP_001362270.1:p.Arg440=
NM_001375342.1:c.1294A>C	NP_001362271.1:p.Arg432=
NM_001375343.1:c.1417A>C	NP_001362272.1:p.Arg473=
NM_001375344.1:c.1360A>C	NP_001362273.1:p.Arg454=
NM_001375345.1:c.1231A>C	NP_001362274.1:p.Arg411=
NM_001375346.1:c.1255A>C	NP_001362275.1:p.Arg419=
NM_001375347.1:c.1234A>C	NP_001362276.1:p.Arg412=
NM_001375348.1:c.877A>C	NP_001362277.1:p.Arg293=
NM_001375349.1:c.1012A>C	NP_001362278.1:p.Arg338=
NM_001375350.1:c.901A>C	NP_001362279.1:p.Arg301=
NM_198904.3:c.1321A>C	NP_944494.1:p.Arg441=
NM_198904.4:c.1321A>C MANE Select	NP_944494.1:p.Arg441=