Canonical Allele Identifier: CA362185021

Gene: GABRG2

Linked Data

• ClinVar Variation Id: 1426255
• ClinVar RCV Id: RCV001931233
• dbSNP Id: rs2113370519
• MyVariant Identifiers: chr5:g.161530922A>G (hg19) ; chr5:g.162103916A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162103916A>G , CM000667.2:g.162103916A>G	GRCh38
NC_000005.9:g.161530922A>G , CM000667.1:g.161530922A>G	GRCh37
NC_000005.8:g.161463500A>G	NCBI36
NG_009290.1:g.41275A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.621A>G
ENST00000361925.9:c.779A>G	ENSP00000354651.5:p.Tyr260Cys
ENST00000522053.2:n.550A>G
ENST00000523372.2:c.742A>G
ENST00000638552.1:c.374A>G	ENSP00000491763.1:p.Tyr125Cys
ENST00000638660.1:c.374A>G	ENSP00000492869.1:p.Tyr125Cys
ENST00000638772.1:c.659A>G	ENSP00000491557.1:p.Tyr220Cys
ENST00000638782.1:n.721A>G
ENST00000638877.1:c.536A>G
ENST00000639046.1:c.50A>G	ENSP00000492659.1:p.Tyr17Cys
ENST00000639111.2:c.659A>G	ENSP00000492125.2:p.Tyr220Cys
ENST00000639213.2:c.659A>G MANE Select	ENSP00000491909.2:p.Tyr220Cys
ENST00000639278.1:c.587A>G	ENSP00000491958.1:p.Tyr196Cys
ENST00000639384.1:c.659A>G	ENSP00000491240.1:p.Tyr220Cys
ENST00000639424.1:c.107+35810A>G	ENSP00000491245.1:n.107+35810A>G
ENST00000639683.1:c.593A>G	ENSP00000492581.1:p.Tyr198Cys
ENST00000639975.1:c.593A>G	ENSP00000492096.1:p.Tyr198Cys
ENST00000640574.1:c.374A>G	ENSP00000491582.1:p.Tyr125Cys
ENST00000640739.1:n.3190A>G
ENST00000640910.1:c.97A>G
ENST00000640985.1:c.572A>G	ENSP00000492293.1:p.Tyr191Cys
ENST00000641017.1:c.659A>G	ENSP00000493461.1:p.Tyr220Cys
ENST00000356592.7:c.659A>G	ENSP00000349000.3:p.Tyr220Cys
ENST00000361925.8:c.659A>G	ENSP00000354651.4:p.Tyr220Cys
ENST00000414552.6:c.779A>G	ENSP00000410732.2:p.Tyr260Cys
ENST00000522053.1:c.374A>G	ENSP00000430182.1:p.Tyr125Cys
ENST00000522990.5:c.*261A>G	ENSP00000430732.1:n.*261A>G
ENST00000523372.1:c.780A>G	ENSP00000430124.1:n.780A>G
NM_000816.3:c.659A>G	NP_000807.2:p.Tyr220Cys
NM_198903.2:c.779A>G	NP_944493.2:p.Tyr260Cys
NM_198904.2:c.659A>G	NP_944494.1:p.Tyr220Cys
NM_001375339.1:c.650A>G	NP_001362268.1:p.Tyr217Cys
NM_001375340.1:c.659A>G	NP_001362269.1:p.Tyr220Cys
NM_001375341.1:c.659A>G	NP_001362270.1:p.Tyr220Cys
NM_001375342.1:c.659A>G	NP_001362271.1:p.Tyr220Cys
NM_001375343.1:c.779A>G	NP_001362272.1:p.Tyr260Cys
NM_001375344.1:c.659A>G	NP_001362273.1:p.Tyr220Cys
NM_001375345.1:c.593A>G	NP_001362274.1:p.Tyr198Cys
NM_001375346.1:c.593A>G	NP_001362275.1:p.Tyr198Cys
NM_001375347.1:c.572A>G	NP_001362276.1:p.Tyr191Cys
NM_001375348.1:c.239A>G	NP_001362277.1:p.Tyr80Cys
NM_001375349.1:c.374A>G	NP_001362278.1:p.Tyr125Cys
NM_001375350.1:c.239A>G	NP_001362279.1:p.Tyr80Cys
NM_198904.3:c.659A>G	NP_944494.1:p.Tyr220Cys
NM_198904.4:c.659A>G MANE Select	NP_944494.1:p.Tyr220Cys