Canonical Allele Identifier: CA362184029

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161580319C>G (hg19) ; chr5:g.162153313C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153313C>G , CM000667.2:g.162153313C>G	GRCh38
NC_000005.9:g.161580319C>G , CM000667.1:g.161580319C>G	GRCh37
NC_000005.8:g.161512897C>G	NCBI36
NG_009290.1:g.90672C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1374C>G
ENST00000361925.9:c.1469C>G	ENSP00000354651.5:p.Pro490Arg
ENST00000523372.2:c.1432C>G
ENST00000638253.1:n.627C>G
ENST00000638552.1:c.1064C>G	ENSP00000491763.1:p.Pro355Arg
ENST00000638660.1:c.1088C>G	ENSP00000492869.1:p.Pro363Arg
ENST00000638772.1:c.*3970C>G	ENSP00000491557.1:n.*3970C>G
ENST00000638877.1:c.1250C>G
ENST00000639046.1:c.740C>G	ENSP00000492659.1:p.Pro247Arg
ENST00000639111.2:c.1349C>G	ENSP00000492125.2:p.Pro450Arg
ENST00000639213.2:c.1373C>G MANE Select	ENSP00000491909.2:p.Pro458Arg
ENST00000639278.1:c.2036C>G	ENSP00000491958.1:n.2036C>G
ENST00000639384.1:c.*1554C>G	ENSP00000491240.1:n.*1554C>G
ENST00000639424.1:c.*573C>G	ENSP00000491245.1:n.*573C>G
ENST00000639683.1:c.1307C>G	ENSP00000492581.1:p.Pro436Arg
ENST00000639975.1:c.1283C>G	ENSP00000492096.1:p.Pro428Arg
ENST00000640500.1:n.647C>G
ENST00000640739.1:n.6320C>G
ENST00000640910.1:c.811C>G
ENST00000640985.1:c.1286C>G	ENSP00000492293.1:p.Pro429Arg
ENST00000641017.1:c.1442C>G	ENSP00000493461.1:p.Pro481Arg
ENST00000356592.7:c.1373C>G	ENSP00000349000.3:p.Pro458Arg
ENST00000361925.8:c.1349C>G	ENSP00000354651.4:p.Pro450Arg
ENST00000414552.6:c.1493C>G	ENSP00000410732.2:p.Pro498Arg
ENST00000522990.5:c.*951C>G	ENSP00000430732.1:n.*951C>G
ENST00000523372.1:c.1470C>G	ENSP00000430124.1:n.1470C>G
NM_000816.3:c.1349C>G	NP_000807.2:p.Pro450Arg
NM_198903.2:c.1493C>G	NP_944493.2:p.Pro498Arg
NM_198904.2:c.1373C>G	NP_944494.1:p.Pro458Arg
NM_001375339.1:c.1364C>G	NP_001362268.1:p.Pro455Arg
NM_001375340.1:c.*207C>G	NP_001362269.1:n.*207C>G
NM_001375341.1:c.1370C>G	NP_001362270.1:p.Pro457Arg
NM_001375342.1:c.1346C>G	NP_001362271.1:p.Pro449Arg
NM_001375343.1:c.1469C>G	NP_001362272.1:p.Pro490Arg
NM_001375344.1:c.1412C>G	NP_001362273.1:p.Pro471Arg
NM_001375345.1:c.1283C>G	NP_001362274.1:p.Pro428Arg
NM_001375346.1:c.1307C>G	NP_001362275.1:p.Pro436Arg
NM_001375347.1:c.1286C>G	NP_001362276.1:p.Pro429Arg
NM_001375348.1:c.929C>G	NP_001362277.1:p.Pro310Arg
NM_001375349.1:c.1064C>G	NP_001362278.1:p.Pro355Arg
NM_001375350.1:c.953C>G	NP_001362279.1:p.Pro318Arg
NM_198904.3:c.1373C>G	NP_944494.1:p.Pro458Arg
NM_198904.4:c.1373C>G MANE Select	NP_944494.1:p.Pro458Arg