Canonical Allele Identifier: CA362185107

Gene: GABRG2

Linked Data

• dbSNP Id: rs1761620462
• MyVariant Identifiers: chr5:g.161530961G>A (hg19) ; chr5:g.162103955G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162103955G>A , CM000667.2:g.162103955G>A	GRCh38
NC_000005.9:g.161530961G>A , CM000667.1:g.161530961G>A	GRCh37
NC_000005.8:g.161463539G>A	NCBI36
NG_009290.1:g.41314G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000356592.8:c.660G>A
ENST00000361925.9:c.818G>A	ENSP00000354651.5:p.Arg273Lys
ENST00000522053.2:n.589G>A
ENST00000523372.2:c.781G>A
ENST00000638552.1:c.413G>A	ENSP00000491763.1:p.Arg138Lys
ENST00000638660.1:c.413G>A	ENSP00000492869.1:p.Arg138Lys
ENST00000638772.1:c.698G>A	ENSP00000491557.1:p.Arg233Lys
ENST00000638782.1:n.760G>A
ENST00000638877.1:c.575G>A
ENST00000639046.1:c.89G>A	ENSP00000492659.1:p.Arg30Lys
ENST00000639111.2:c.698G>A	ENSP00000492125.2:p.Arg233Lys
ENST00000639213.2:c.698G>A MANE Select	ENSP00000491909.2:p.Arg233Lys
ENST00000639278.1:c.626G>A	ENSP00000491958.1:p.Arg209Lys
ENST00000639384.1:c.698G>A	ENSP00000491240.1:p.Arg233Lys
ENST00000639424.1:c.107+35849G>A	ENSP00000491245.1:n.107+35849G>A
ENST00000639683.1:c.632G>A	ENSP00000492581.1:p.Arg211Lys
ENST00000639975.1:c.632G>A	ENSP00000492096.1:p.Arg211Lys
ENST00000640574.1:c.413G>A	ENSP00000491582.1:p.Arg138Lys
ENST00000640739.1:n.3229G>A
ENST00000640910.1:c.136G>A
ENST00000640985.1:c.611G>A	ENSP00000492293.1:p.Arg204Lys
ENST00000641017.1:c.698G>A	ENSP00000493461.1:p.Arg233Lys
ENST00000356592.7:c.698G>A	ENSP00000349000.3:p.Arg233Lys
ENST00000361925.8:c.698G>A	ENSP00000354651.4:p.Arg233Lys
ENST00000414552.6:c.818G>A	ENSP00000410732.2:p.Arg273Lys
ENST00000522053.1:c.413G>A	ENSP00000430182.1:p.Arg138Lys
ENST00000522990.5:c.*300G>A	ENSP00000430732.1:n.*300G>A
ENST00000523372.1:c.819G>A	ENSP00000430124.1:n.819G>A
NM_000816.3:c.698G>A	NP_000807.2:p.Arg233Lys
NM_198903.2:c.818G>A	NP_944493.2:p.Arg273Lys
NM_198904.2:c.698G>A	NP_944494.1:p.Arg233Lys
NM_001375339.1:c.689G>A	NP_001362268.1:p.Arg230Lys
NM_001375340.1:c.698G>A	NP_001362269.1:p.Arg233Lys
NM_001375341.1:c.698G>A	NP_001362270.1:p.Arg233Lys
NM_001375342.1:c.698G>A	NP_001362271.1:p.Arg233Lys
NM_001375343.1:c.818G>A	NP_001362272.1:p.Arg273Lys
NM_001375344.1:c.698G>A	NP_001362273.1:p.Arg233Lys
NM_001375345.1:c.632G>A	NP_001362274.1:p.Arg211Lys
NM_001375346.1:c.632G>A	NP_001362275.1:p.Arg211Lys
NM_001375347.1:c.611G>A	NP_001362276.1:p.Arg204Lys
NM_001375348.1:c.278G>A	NP_001362277.1:p.Arg93Lys
NM_001375349.1:c.413G>A	NP_001362278.1:p.Arg138Lys
NM_001375350.1:c.278G>A	NP_001362279.1:p.Arg93Lys
NM_198904.3:c.698G>A	NP_944494.1:p.Arg233Lys
NM_198904.4:c.698G>A MANE Select	NP_944494.1:p.Arg233Lys