Canonical Allele Identifier: CA362183616
Gene: GABRG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162153215T>G , CM000667.2:g.162153215T>G GRCh38
NC_000005.9:g.161580221T>G , CM000667.1:g.161580221T>G GRCh37
NC_000005.8:g.161512799T>G NCBI36
NG_009290.1:g.90574T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.1276T>G
ENST00000361925.9:c.1371T>G ENSP00000354651.5:p.Phe457Leu
ENST00000523372.2:c.1334T>G
ENST00000638253.1:n.529T>G
ENST00000638552.1:c.966T>G ENSP00000491763.1:p.Phe322Leu
ENST00000638660.1:c.990T>G ENSP00000492869.1:p.Phe330Leu
ENST00000638772.1:c.*3872T>G ENSP00000491557.1:n.*3872T>G
ENST00000638877.1:c.1152T>G
ENST00000639046.1:c.642T>G ENSP00000492659.1:p.Phe214Leu
ENST00000639111.2:c.1251T>G ENSP00000492125.2:p.Phe417Leu
ENST00000639213.2:c.1275T>G MANE Select ENSP00000491909.2:p.Phe425Leu
ENST00000639278.1:c.1938T>G ENSP00000491958.1:n.1938T>G
ENST00000639384.1:c.*1456T>G ENSP00000491240.1:n.*1456T>G
ENST00000639424.1:c.*475T>G ENSP00000491245.1:n.*475T>G
ENST00000639683.1:c.1209T>G ENSP00000492581.1:p.Phe403Leu
ENST00000639975.1:c.1185T>G ENSP00000492096.1:p.Phe395Leu
ENST00000640500.1:n.549T>G
ENST00000640739.1:n.6222T>G
ENST00000640910.1:c.713T>G
ENST00000640985.1:c.1188T>G ENSP00000492293.1:p.Phe396Leu
ENST00000641017.1:c.1344T>G ENSP00000493461.1:p.Phe448Leu
ENST00000356592.7:c.1275T>G ENSP00000349000.3:p.Phe425Leu
ENST00000361925.8:c.1251T>G ENSP00000354651.4:p.Phe417Leu
ENST00000414552.6:c.1395T>G ENSP00000410732.2:p.Phe465Leu
ENST00000522990.5:c.*853T>G ENSP00000430732.1:n.*853T>G
ENST00000523372.1:c.1372T>G ENSP00000430124.1:n.1372T>G
NM_000816.3:c.1251T>G NP_000807.2:p.Phe417Leu
NM_198903.2:c.1395T>G NP_944493.2:p.Phe465Leu
NM_198904.2:c.1275T>G NP_944494.1:p.Phe425Leu
NM_001375339.1:c.1266T>G NP_001362268.1:p.Phe422Leu
NM_001375340.1:c.*109T>G NP_001362269.1:n.*109T>G
NM_001375341.1:c.1272T>G NP_001362270.1:p.Phe424Leu
NM_001375342.1:c.1248T>G NP_001362271.1:p.Phe416Leu
NM_001375343.1:c.1371T>G NP_001362272.1:p.Phe457Leu
NM_001375344.1:c.1314T>G NP_001362273.1:p.Phe438Leu
NM_001375345.1:c.1185T>G NP_001362274.1:p.Phe395Leu
NM_001375346.1:c.1209T>G NP_001362275.1:p.Phe403Leu
NM_001375347.1:c.1188T>G NP_001362276.1:p.Phe396Leu
NM_001375348.1:c.831T>G NP_001362277.1:p.Phe277Leu
NM_001375349.1:c.966T>G NP_001362278.1:p.Phe322Leu
NM_001375350.1:c.855T>G NP_001362279.1:p.Phe285Leu
NM_198904.3:c.1275T>G NP_944494.1:p.Phe425Leu
NM_198904.4:c.1275T>G MANE Select NP_944494.1:p.Phe425Leu