Canonical Allele Identifier: CA447691561

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161580134C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153128C>T , CM000667.2:g.162153128C>T	GRCh38
NC_000005.9:g.161580134C>T , CM000667.1:g.161580134C>T	GRCh37
NC_000005.8:g.161512712C>T	NCBI36
NG_009290.1:g.90487C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1189C>T
ENST00000361925.9:c.1284C>T	ENSP00000354651.5:p.Thr428=
ENST00000523372.2:c.1247C>T
ENST00000638253.1:n.442C>T
ENST00000638552.1:c.879C>T	ENSP00000491763.1:p.Thr293=
ENST00000638660.1:c.903C>T	ENSP00000492869.1:p.Thr301=
ENST00000638772.1:c.*3785C>T	ENSP00000491557.1:n.*3785C>T
ENST00000638877.1:c.1065C>T
ENST00000639046.1:c.555C>T	ENSP00000492659.1:p.Thr185=
ENST00000639111.2:c.1164C>T	ENSP00000492125.2:p.Thr388=
ENST00000639213.2:c.1188C>T MANE Select	ENSP00000491909.2:p.Thr396=
ENST00000639278.1:c.1851C>T	ENSP00000491958.1:n.1851C>T
ENST00000639384.1:c.*1369C>T	ENSP00000491240.1:n.*1369C>T
ENST00000639424.1:c.*388C>T	ENSP00000491245.1:n.*388C>T
ENST00000639683.1:c.1122C>T	ENSP00000492581.1:p.Thr374=
ENST00000639975.1:c.1098C>T	ENSP00000492096.1:p.Thr366=
ENST00000640500.1:n.462C>T
ENST00000640739.1:n.6135C>T
ENST00000640910.1:c.626C>T
ENST00000640985.1:c.1101C>T	ENSP00000492293.1:p.Thr367=
ENST00000641017.1:c.1257C>T	ENSP00000493461.1:p.Thr419=
ENST00000356592.7:c.1188C>T	ENSP00000349000.3:p.Thr396=
ENST00000361925.8:c.1164C>T	ENSP00000354651.4:p.Thr388=
ENST00000414552.6:c.1308C>T	ENSP00000410732.2:p.Thr436=
ENST00000522990.5:c.*766C>T	ENSP00000430732.1:n.*766C>T
ENST00000523372.1:c.1285C>T	ENSP00000430124.1:n.1285C>T
NM_000816.3:c.1164C>T	NP_000807.2:p.Thr388=
NM_198903.2:c.1308C>T	NP_944493.2:p.Thr436=
NM_198904.2:c.1188C>T	NP_944494.1:p.Thr396=
NM_001375339.1:c.1179C>T	NP_001362268.1:p.Thr393=
NM_001375340.1:c.*22C>T	NP_001362269.1:n.*22C>T
NM_001375341.1:c.1185C>T	NP_001362270.1:p.Thr395=
NM_001375342.1:c.1161C>T	NP_001362271.1:p.Thr387=
NM_001375343.1:c.1284C>T	NP_001362272.1:p.Thr428=
NM_001375344.1:c.1227C>T	NP_001362273.1:p.Thr409=
NM_001375345.1:c.1098C>T	NP_001362274.1:p.Thr366=
NM_001375346.1:c.1122C>T	NP_001362275.1:p.Thr374=
NM_001375347.1:c.1101C>T	NP_001362276.1:p.Thr367=
NM_001375348.1:c.744C>T	NP_001362277.1:p.Thr248=
NM_001375349.1:c.879C>T	NP_001362278.1:p.Thr293=
NM_001375350.1:c.768C>T	NP_001362279.1:p.Thr256=
NM_198904.3:c.1188C>T	NP_944494.1:p.Thr396=
NM_198904.4:c.1188C>T MANE Select	NP_944494.1:p.Thr396=