Canonical Allele Identifier: CA1596382211
Gene: GABRG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162153296T= , CM000667.2:g.162153296T= GRCh38
NC_000005.9:g.161580302T= , CM000667.1:g.161580302T= GRCh37
NC_000005.8:g.161512880T= NCBI36
NG_009290.1:g.90655T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.1357T=
ENST00000361925.9:c.1452T= ENSP00000354651.5:p.Tyr484=
ENST00000523372.2:c.1415T=
ENST00000638253.1:n.610T=
ENST00000638552.1:c.1047T= ENSP00000491763.1:p.Tyr349=
ENST00000638660.1:c.1071T= ENSP00000492869.1:p.Tyr357=
ENST00000638772.1:c.*3953T= ENSP00000491557.1:n.*3953T=
ENST00000638877.1:c.1233T=
ENST00000639046.1:c.723T= ENSP00000492659.1:p.Tyr241=
ENST00000639111.2:c.1332T= ENSP00000492125.2:p.Tyr444=
ENST00000639213.2:c.1356T= MANE Select ENSP00000491909.2:p.Tyr452=
ENST00000639278.1:c.2019T= ENSP00000491958.1:n.2019T=
ENST00000639384.1:c.*1537T= ENSP00000491240.1:n.*1537T=
ENST00000639424.1:c.*556T= ENSP00000491245.1:n.*556T=
ENST00000639683.1:c.1290T= ENSP00000492581.1:p.Tyr430=
ENST00000639975.1:c.1266T= ENSP00000492096.1:p.Tyr422=
ENST00000640500.1:n.630T=
ENST00000640739.1:n.6303T=
ENST00000640910.1:c.794T=
ENST00000640985.1:c.1269T= ENSP00000492293.1:p.Tyr423=
ENST00000641017.1:c.1425T= ENSP00000493461.1:p.Tyr475=
ENST00000356592.7:c.1356T= ENSP00000349000.3:p.Tyr452=
ENST00000361925.8:c.1332T= ENSP00000354651.4:p.Tyr444=
ENST00000414552.6:c.1476T= ENSP00000410732.2:p.Tyr492=
ENST00000522990.5:c.*934T= ENSP00000430732.1:n.*934T=
ENST00000523372.1:c.1453T= ENSP00000430124.1:n.1453T=
NM_000816.3:c.1332T= NP_000807.2:p.Tyr444=
NM_198903.2:c.1476T= NP_944493.2:p.Tyr492=
NM_198904.2:c.1356T= NP_944494.1:p.Tyr452=
NM_001375339.1:c.1347T= NP_001362268.1:p.Tyr449=
NM_001375340.1:c.*190T= NP_001362269.1:n.*190T=
NM_001375341.1:c.1353T= NP_001362270.1:p.Tyr451=
NM_001375342.1:c.1329T= NP_001362271.1:p.Tyr443=
NM_001375343.1:c.1452T= NP_001362272.1:p.Tyr484=
NM_001375344.1:c.1395T= NP_001362273.1:p.Tyr465=
NM_001375345.1:c.1266T= NP_001362274.1:p.Tyr422=
NM_001375346.1:c.1290T= NP_001362275.1:p.Tyr430=
NM_001375347.1:c.1269T= NP_001362276.1:p.Tyr423=
NM_001375348.1:c.912T= NP_001362277.1:p.Tyr304=
NM_001375349.1:c.1047T= NP_001362278.1:p.Tyr349=
NM_001375350.1:c.936T= NP_001362279.1:p.Tyr312=
NM_198904.3:c.1356T= NP_944494.1:p.Tyr452=
NM_198904.4:c.1356T= MANE Select NP_944494.1:p.Tyr452=