Canonical Allele Identifier: CA447609975

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161530960A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162103954A>C , CM000667.2:g.162103954A>C	GRCh38
NC_000005.9:g.161530960A>C , CM000667.1:g.161530960A>C	GRCh37
NC_000005.8:g.161463538A>C	NCBI36
NG_009290.1:g.41313A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000356592.8:c.659A>C
ENST00000361925.9:c.817A>C	ENSP00000354651.5:p.Arg273=
ENST00000522053.2:n.588A>C
ENST00000523372.2:c.780A>C
ENST00000638552.1:c.412A>C	ENSP00000491763.1:p.Arg138=
ENST00000638660.1:c.412A>C	ENSP00000492869.1:p.Arg138=
ENST00000638772.1:c.697A>C	ENSP00000491557.1:p.Arg233=
ENST00000638782.1:n.759A>C
ENST00000638877.1:c.574A>C
ENST00000639046.1:c.88A>C	ENSP00000492659.1:p.Arg30=
ENST00000639111.2:c.697A>C	ENSP00000492125.2:p.Arg233=
ENST00000639213.2:c.697A>C MANE Select	ENSP00000491909.2:p.Arg233=
ENST00000639278.1:c.625A>C	ENSP00000491958.1:p.Arg209=
ENST00000639384.1:c.697A>C	ENSP00000491240.1:p.Arg233=
ENST00000639424.1:c.107+35848A>C	ENSP00000491245.1:n.107+35848A>C
ENST00000639683.1:c.631A>C	ENSP00000492581.1:p.Arg211=
ENST00000639975.1:c.631A>C	ENSP00000492096.1:p.Arg211=
ENST00000640574.1:c.412A>C	ENSP00000491582.1:p.Arg138=
ENST00000640739.1:n.3228A>C
ENST00000640910.1:c.135A>C
ENST00000640985.1:c.610A>C	ENSP00000492293.1:p.Arg204=
ENST00000641017.1:c.697A>C	ENSP00000493461.1:p.Arg233=
ENST00000356592.7:c.697A>C	ENSP00000349000.3:p.Arg233=
ENST00000361925.8:c.697A>C	ENSP00000354651.4:p.Arg233=
ENST00000414552.6:c.817A>C	ENSP00000410732.2:p.Arg273=
ENST00000522053.1:c.412A>C	ENSP00000430182.1:p.Arg138=
ENST00000522990.5:c.*299A>C	ENSP00000430732.1:n.*299A>C
ENST00000523372.1:c.818A>C	ENSP00000430124.1:n.818A>C
NM_000816.3:c.697A>C	NP_000807.2:p.Arg233=
NM_198903.2:c.817A>C	NP_944493.2:p.Arg273=
NM_198904.2:c.697A>C	NP_944494.1:p.Arg233=
NM_001375339.1:c.688A>C	NP_001362268.1:p.Arg230=
NM_001375340.1:c.697A>C	NP_001362269.1:p.Arg233=
NM_001375341.1:c.697A>C	NP_001362270.1:p.Arg233=
NM_001375342.1:c.697A>C	NP_001362271.1:p.Arg233=
NM_001375343.1:c.817A>C	NP_001362272.1:p.Arg273=
NM_001375344.1:c.697A>C	NP_001362273.1:p.Arg233=
NM_001375345.1:c.631A>C	NP_001362274.1:p.Arg211=
NM_001375346.1:c.631A>C	NP_001362275.1:p.Arg211=
NM_001375347.1:c.610A>C	NP_001362276.1:p.Arg204=
NM_001375348.1:c.277A>C	NP_001362277.1:p.Arg93=
NM_001375349.1:c.412A>C	NP_001362278.1:p.Arg138=
NM_001375350.1:c.277A>C	NP_001362279.1:p.Arg93=
NM_198904.3:c.697A>C	NP_944494.1:p.Arg233=
NM_198904.4:c.697A>C MANE Select	NP_944494.1:p.Arg233=