Canonical Allele Identifier: CA447691898

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161580266G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153260G>T , CM000667.2:g.162153260G>T	GRCh38
NC_000005.9:g.161580266G>T , CM000667.1:g.161580266G>T	GRCh37
NC_000005.8:g.161512844G>T	NCBI36
NG_009290.1:g.90619G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1321G>T
ENST00000361925.9:c.1416G>T	ENSP00000354651.5:p.Gly472=
ENST00000523372.2:c.1379G>T
ENST00000638253.1:n.574G>T
ENST00000638552.1:c.1011G>T	ENSP00000491763.1:p.Gly337=
ENST00000638660.1:c.1035G>T	ENSP00000492869.1:p.Gly345=
ENST00000638772.1:c.*3917G>T	ENSP00000491557.1:n.*3917G>T
ENST00000638877.1:c.1197G>T
ENST00000639046.1:c.687G>T	ENSP00000492659.1:p.Gly229=
ENST00000639111.2:c.1296G>T	ENSP00000492125.2:p.Gly432=
ENST00000639213.2:c.1320G>T MANE Select	ENSP00000491909.2:p.Gly440=
ENST00000639278.1:c.1983G>T	ENSP00000491958.1:n.1983G>T
ENST00000639384.1:c.*1501G>T	ENSP00000491240.1:n.*1501G>T
ENST00000639424.1:c.*520G>T	ENSP00000491245.1:n.*520G>T
ENST00000639683.1:c.1254G>T	ENSP00000492581.1:p.Gly418=
ENST00000639975.1:c.1230G>T	ENSP00000492096.1:p.Gly410=
ENST00000640500.1:n.594G>T
ENST00000640739.1:n.6267G>T
ENST00000640910.1:c.758G>T
ENST00000640985.1:c.1233G>T	ENSP00000492293.1:p.Gly411=
ENST00000641017.1:c.1389G>T	ENSP00000493461.1:p.Gly463=
ENST00000356592.7:c.1320G>T	ENSP00000349000.3:p.Gly440=
ENST00000361925.8:c.1296G>T	ENSP00000354651.4:p.Gly432=
ENST00000414552.6:c.1440G>T	ENSP00000410732.2:p.Gly480=
ENST00000522990.5:c.*898G>T	ENSP00000430732.1:n.*898G>T
ENST00000523372.1:c.1417G>T	ENSP00000430124.1:n.1417G>T
NM_000816.3:c.1296G>T	NP_000807.2:p.Gly432=
NM_198903.2:c.1440G>T	NP_944493.2:p.Gly480=
NM_198904.2:c.1320G>T	NP_944494.1:p.Gly440=
NM_001375339.1:c.1311G>T	NP_001362268.1:p.Gly437=
NM_001375340.1:c.*154G>T	NP_001362269.1:n.*154G>T
NM_001375341.1:c.1317G>T	NP_001362270.1:p.Gly439=
NM_001375342.1:c.1293G>T	NP_001362271.1:p.Gly431=
NM_001375343.1:c.1416G>T	NP_001362272.1:p.Gly472=
NM_001375344.1:c.1359G>T	NP_001362273.1:p.Gly453=
NM_001375345.1:c.1230G>T	NP_001362274.1:p.Gly410=
NM_001375346.1:c.1254G>T	NP_001362275.1:p.Gly418=
NM_001375347.1:c.1233G>T	NP_001362276.1:p.Gly411=
NM_001375348.1:c.876G>T	NP_001362277.1:p.Gly292=
NM_001375349.1:c.1011G>T	NP_001362278.1:p.Gly337=
NM_001375350.1:c.900G>T	NP_001362279.1:p.Gly300=
NM_198904.3:c.1320G>T	NP_944494.1:p.Gly440=
NM_198904.4:c.1320G>T MANE Select	NP_944494.1:p.Gly440=