Canonical Allele Identifier: CA362183741

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161580249G>T (hg19) ; chr5:g.162153243G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153243G>T , CM000667.2:g.162153243G>T	GRCh38
NC_000005.9:g.161580249G>T , CM000667.1:g.161580249G>T	GRCh37
NC_000005.8:g.161512827G>T	NCBI36
NG_009290.1:g.90602G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1304G>T
ENST00000361925.9:c.1399G>T	ENSP00000354651.5:p.Gly467Ter
ENST00000523372.2:c.1362G>T
ENST00000638253.1:n.557G>T
ENST00000638552.1:c.994G>T	ENSP00000491763.1:p.Gly332Ter
ENST00000638660.1:c.1018G>T	ENSP00000492869.1:p.Gly340Ter
ENST00000638772.1:c.*3900G>T	ENSP00000491557.1:n.*3900G>T
ENST00000638877.1:c.1180G>T
ENST00000639046.1:c.670G>T	ENSP00000492659.1:p.Gly224Ter
ENST00000639111.2:c.1279G>T	ENSP00000492125.2:p.Gly427Ter
ENST00000639213.2:c.1303G>T MANE Select	ENSP00000491909.2:p.Gly435Ter
ENST00000639278.1:c.1966G>T	ENSP00000491958.1:n.1966G>T
ENST00000639384.1:c.*1484G>T	ENSP00000491240.1:n.*1484G>T
ENST00000639424.1:c.*503G>T	ENSP00000491245.1:n.*503G>T
ENST00000639683.1:c.1237G>T	ENSP00000492581.1:p.Gly413Ter
ENST00000639975.1:c.1213G>T	ENSP00000492096.1:p.Gly405Ter
ENST00000640500.1:n.577G>T
ENST00000640739.1:n.6250G>T
ENST00000640910.1:c.741G>T
ENST00000640985.1:c.1216G>T	ENSP00000492293.1:p.Gly406Ter
ENST00000641017.1:c.1372G>T	ENSP00000493461.1:p.Gly458Ter
ENST00000356592.7:c.1303G>T	ENSP00000349000.3:p.Gly435Ter
ENST00000361925.8:c.1279G>T	ENSP00000354651.4:p.Gly427Ter
ENST00000414552.6:c.1423G>T	ENSP00000410732.2:p.Gly475Ter
ENST00000522990.5:c.*881G>T	ENSP00000430732.1:n.*881G>T
ENST00000523372.1:c.1400G>T	ENSP00000430124.1:n.1400G>T
NM_000816.3:c.1279G>T	NP_000807.2:p.Gly427Ter
NM_198903.2:c.1423G>T	NP_944493.2:p.Gly475Ter
NM_198904.2:c.1303G>T	NP_944494.1:p.Gly435Ter
NM_001375339.1:c.1294G>T	NP_001362268.1:p.Gly432Ter
NM_001375340.1:c.*137G>T	NP_001362269.1:n.*137G>T
NM_001375341.1:c.1300G>T	NP_001362270.1:p.Gly434Ter
NM_001375342.1:c.1276G>T	NP_001362271.1:p.Gly426Ter
NM_001375343.1:c.1399G>T	NP_001362272.1:p.Gly467Ter
NM_001375344.1:c.1342G>T	NP_001362273.1:p.Gly448Ter
NM_001375345.1:c.1213G>T	NP_001362274.1:p.Gly405Ter
NM_001375346.1:c.1237G>T	NP_001362275.1:p.Gly413Ter
NM_001375347.1:c.1216G>T	NP_001362276.1:p.Gly406Ter
NM_001375348.1:c.859G>T	NP_001362277.1:p.Gly287Ter
NM_001375349.1:c.994G>T	NP_001362278.1:p.Gly332Ter
NM_001375350.1:c.883G>T	NP_001362279.1:p.Gly295Ter
NM_198904.3:c.1303G>T	NP_944494.1:p.Gly435Ter
NM_198904.4:c.1303G>T MANE Select	NP_944494.1:p.Gly435Ter