Canonical Allele Identifier: CA447610337

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161576280G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162149274G>C , CM000667.2:g.162149274G>C	GRCh38
NC_000005.9:g.161576280G>C , CM000667.1:g.161576280G>C	GRCh37
NC_000005.8:g.161508858G>C	NCBI36
NG_009290.1:g.86633G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1090G>C
ENST00000361925.9:c.1209G>C	ENSP00000354651.5:p.Arg403=
ENST00000523372.2:c.1172G>C
ENST00000638253.1:n.343G>C
ENST00000638552.1:c.804G>C	ENSP00000491763.1:p.Arg268=
ENST00000638660.1:c.804G>C	ENSP00000492869.1:p.Arg268=
ENST00000638772.1:c.1089G>C	ENSP00000491557.1:p.Arg363=
ENST00000638877.1:c.966G>C
ENST00000639046.1:c.480G>C	ENSP00000492659.1:p.Arg160=
ENST00000639111.2:c.1089G>C	ENSP00000492125.2:p.Arg363=
ENST00000639213.2:c.1089G>C MANE Select	ENSP00000491909.2:p.Arg363=
ENST00000639278.1:c.1017G>C	ENSP00000491958.1:p.Arg339=
ENST00000639384.1:c.1089G>C	ENSP00000491240.1:p.Arg363=
ENST00000639424.1:c.*289G>C	ENSP00000491245.1:n.*289G>C
ENST00000639683.1:c.1023G>C	ENSP00000492581.1:p.Arg341=
ENST00000639975.1:c.1023G>C	ENSP00000492096.1:p.Arg341=
ENST00000640500.1:n.387G>C
ENST00000640574.1:c.804G>C	ENSP00000491582.1:p.Arg268=
ENST00000640739.1:n.3620G>C
ENST00000640910.1:c.527G>C
ENST00000640985.1:c.1002G>C	ENSP00000492293.1:p.Arg334=
ENST00000641017.1:c.1089G>C	ENSP00000493461.1:p.Arg363=
ENST00000356592.7:c.1089G>C	ENSP00000349000.3:p.Arg363=
ENST00000361925.8:c.1089G>C	ENSP00000354651.4:p.Arg363=
ENST00000414552.6:c.1209G>C	ENSP00000410732.2:p.Arg403=
ENST00000522990.5:c.*691G>C	ENSP00000430732.1:n.*691G>C
ENST00000523372.1:c.1210G>C	ENSP00000430124.1:n.1210G>C
NM_000816.3:c.1089G>C	NP_000807.2:p.Arg363=
NM_198903.2:c.1209G>C	NP_944493.2:p.Arg403=
NM_198904.2:c.1089G>C	NP_944494.1:p.Arg363=
NM_001375339.1:c.1080G>C	NP_001362268.1:p.Arg360=
NM_001375340.1:c.923-2456G>C	NP_001362269.1:n.923-2456G>C
NM_001375341.1:c.1086G>C	NP_001362270.1:p.Arg362=
NM_001375342.1:c.1086G>C	NP_001362271.1:p.Arg362=
NM_001375343.1:c.1209G>C	NP_001362272.1:p.Arg403=
NM_001375344.1:c.1128G>C	NP_001362273.1:p.Arg376=
NM_001375345.1:c.1023G>C	NP_001362274.1:p.Arg341=
NM_001375346.1:c.1023G>C	NP_001362275.1:p.Arg341=
NM_001375347.1:c.1002G>C	NP_001362276.1:p.Arg334=
NM_001375348.1:c.669G>C	NP_001362277.1:p.Arg223=
NM_001375349.1:c.804G>C	NP_001362278.1:p.Arg268=
NM_001375350.1:c.669G>C	NP_001362279.1:p.Arg223=
NM_198904.3:c.1089G>C	NP_944494.1:p.Arg363=
NM_198904.4:c.1089G>C MANE Select	NP_944494.1:p.Arg363=