Canonical Allele Identifier: CA362183400

Gene: GABRG2

Linked Data

• dbSNP Id: rs1765496647
• MyVariant Identifiers: chr5:g.161580166A>G (hg19) ; chr5:g.162153160A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153160A>G , CM000667.2:g.162153160A>G	GRCh38
NC_000005.9:g.161580166A>G , CM000667.1:g.161580166A>G	GRCh37
NC_000005.8:g.161512744A>G	NCBI36
NG_009290.1:g.90519A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1221A>G
ENST00000361925.9:c.1316A>G	ENSP00000354651.5:p.Glu439Gly
ENST00000523372.2:c.1279A>G
ENST00000638253.1:n.474A>G
ENST00000638552.1:c.911A>G	ENSP00000491763.1:p.Glu304Gly
ENST00000638660.1:c.935A>G	ENSP00000492869.1:p.Glu312Gly
ENST00000638772.1:c.*3817A>G	ENSP00000491557.1:n.*3817A>G
ENST00000638877.1:c.1097A>G
ENST00000639046.1:c.587A>G	ENSP00000492659.1:p.Glu196Gly
ENST00000639111.2:c.1196A>G	ENSP00000492125.2:p.Glu399Gly
ENST00000639213.2:c.1220A>G MANE Select	ENSP00000491909.2:p.Glu407Gly
ENST00000639278.1:c.1883A>G	ENSP00000491958.1:n.1883A>G
ENST00000639384.1:c.*1401A>G	ENSP00000491240.1:n.*1401A>G
ENST00000639424.1:c.*420A>G	ENSP00000491245.1:n.*420A>G
ENST00000639683.1:c.1154A>G	ENSP00000492581.1:p.Glu385Gly
ENST00000639975.1:c.1130A>G	ENSP00000492096.1:p.Glu377Gly
ENST00000640500.1:n.494A>G
ENST00000640739.1:n.6167A>G
ENST00000640910.1:c.658A>G
ENST00000640985.1:c.1133A>G	ENSP00000492293.1:p.Glu378Gly
ENST00000641017.1:c.1289A>G	ENSP00000493461.1:p.Glu430Gly
ENST00000356592.7:c.1220A>G	ENSP00000349000.3:p.Glu407Gly
ENST00000361925.8:c.1196A>G	ENSP00000354651.4:p.Glu399Gly
ENST00000414552.6:c.1340A>G	ENSP00000410732.2:p.Glu447Gly
ENST00000522990.5:c.*798A>G	ENSP00000430732.1:n.*798A>G
ENST00000523372.1:c.1317A>G	ENSP00000430124.1:n.1317A>G
NM_000816.3:c.1196A>G	NP_000807.2:p.Glu399Gly
NM_198903.2:c.1340A>G	NP_944493.2:p.Glu447Gly
NM_198904.2:c.1220A>G	NP_944494.1:p.Glu407Gly
NM_001375339.1:c.1211A>G	NP_001362268.1:p.Glu404Gly
NM_001375340.1:c.*54A>G	NP_001362269.1:n.*54A>G
NM_001375341.1:c.1217A>G	NP_001362270.1:p.Glu406Gly
NM_001375342.1:c.1193A>G	NP_001362271.1:p.Glu398Gly
NM_001375343.1:c.1316A>G	NP_001362272.1:p.Glu439Gly
NM_001375344.1:c.1259A>G	NP_001362273.1:p.Glu420Gly
NM_001375345.1:c.1130A>G	NP_001362274.1:p.Glu377Gly
NM_001375346.1:c.1154A>G	NP_001362275.1:p.Glu385Gly
NM_001375347.1:c.1133A>G	NP_001362276.1:p.Glu378Gly
NM_001375348.1:c.776A>G	NP_001362277.1:p.Glu259Gly
NM_001375349.1:c.911A>G	NP_001362278.1:p.Glu304Gly
NM_001375350.1:c.800A>G	NP_001362279.1:p.Glu267Gly
NM_198904.3:c.1220A>G	NP_944494.1:p.Glu407Gly
NM_198904.4:c.1220A>G MANE Select	NP_944494.1:p.Glu407Gly