Canonical Allele Identifier: CA362184227

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161580360T>G (hg19) ; chr5:g.162153354T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153354T>G , CM000667.2:g.162153354T>G	GRCh38
NC_000005.9:g.161580360T>G , CM000667.1:g.161580360T>G	GRCh37
NC_000005.8:g.161512938T>G	NCBI36
NG_009290.1:g.90713T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1415T>G
ENST00000361925.9:c.1510T>G	ENSP00000354651.5:p.Tyr504Asp
ENST00000523372.2:c.1473T>G
ENST00000638253.1:n.668T>G
ENST00000638552.1:c.1105T>G	ENSP00000491763.1:p.Tyr369Asp
ENST00000638660.1:c.1129T>G	ENSP00000492869.1:p.Tyr377Asp
ENST00000638772.1:c.*4011T>G	ENSP00000491557.1:n.*4011T>G
ENST00000638877.1:c.1291T>G
ENST00000639046.1:c.781T>G	ENSP00000492659.1:p.Tyr261Asp
ENST00000639111.2:c.1390T>G	ENSP00000492125.2:p.Tyr464Asp
ENST00000639213.2:c.1414T>G MANE Select	ENSP00000491909.2:p.Tyr472Asp
ENST00000639278.1:c.2077T>G	ENSP00000491958.1:n.2077T>G
ENST00000639384.1:c.*1595T>G	ENSP00000491240.1:n.*1595T>G
ENST00000639424.1:c.*614T>G	ENSP00000491245.1:n.*614T>G
ENST00000639683.1:c.1348T>G	ENSP00000492581.1:p.Tyr450Asp
ENST00000639975.1:c.1324T>G	ENSP00000492096.1:p.Tyr442Asp
ENST00000640500.1:n.688T>G
ENST00000640739.1:n.6361T>G
ENST00000640910.1:c.852T>G
ENST00000640985.1:c.1327T>G	ENSP00000492293.1:p.Tyr443Asp
ENST00000641017.1:c.1483T>G	ENSP00000493461.1:p.Tyr495Asp
ENST00000356592.7:c.1414T>G	ENSP00000349000.3:p.Tyr472Asp
ENST00000361925.8:c.1390T>G	ENSP00000354651.4:p.Tyr464Asp
ENST00000414552.6:c.1534T>G	ENSP00000410732.2:p.Tyr512Asp
ENST00000522990.5:c.*992T>G	ENSP00000430732.1:n.*992T>G
ENST00000523372.1:c.1511T>G	ENSP00000430124.1:n.1511T>G
NM_000816.3:c.1390T>G	NP_000807.2:p.Tyr464Asp
NM_198903.2:c.1534T>G	NP_944493.2:p.Tyr512Asp
NM_198904.2:c.1414T>G	NP_944494.1:p.Tyr472Asp
NM_001375339.1:c.1405T>G	NP_001362268.1:p.Tyr469Asp
NM_001375340.1:c.*248T>G	NP_001362269.1:n.*248T>G
NM_001375341.1:c.1411T>G	NP_001362270.1:p.Tyr471Asp
NM_001375342.1:c.1387T>G	NP_001362271.1:p.Tyr463Asp
NM_001375343.1:c.1510T>G	NP_001362272.1:p.Tyr504Asp
NM_001375344.1:c.1453T>G	NP_001362273.1:p.Tyr485Asp
NM_001375345.1:c.1324T>G	NP_001362274.1:p.Tyr442Asp
NM_001375346.1:c.1348T>G	NP_001362275.1:p.Tyr450Asp
NM_001375347.1:c.1327T>G	NP_001362276.1:p.Tyr443Asp
NM_001375348.1:c.970T>G	NP_001362277.1:p.Tyr324Asp
NM_001375349.1:c.1105T>G	NP_001362278.1:p.Tyr369Asp
NM_001375350.1:c.994T>G	NP_001362279.1:p.Tyr332Asp
NM_198904.3:c.1414T>G	NP_944494.1:p.Tyr472Asp
NM_198904.4:c.1414T>G MANE Select	NP_944494.1:p.Tyr472Asp