Canonical Allele Identifier: CA1596365183
Gene: GABRG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162103857T= , CM000667.2:g.162103857T= GRCh38
NC_000005.9:g.161530863T= , CM000667.1:g.161530863T= GRCh37
NC_000005.8:g.161463441T= NCBI36
NG_009290.1:g.41216T=

Transcript Alleles

HGVS Amino-acid change
ENST00000356592.8:c.594-32T=
ENST00000361925.9:c.752-32T= ENSP00000354651.5:n.752-32T=
ENST00000522053.2:n.523-32T=
ENST00000523372.2:c.715-32T=
ENST00000638552.1:c.347-32T= ENSP00000491763.1:n.347-32T=
ENST00000638660.1:c.347-32T= ENSP00000492869.1:n.347-32T=
ENST00000638772.1:c.632-32T= ENSP00000491557.1:n.632-32T=
ENST00000638782.1:n.694-32T=
ENST00000638877.1:c.509-32T=
ENST00000639046.1:c.23-32T= ENSP00000492659.1:n.23-32T=
ENST00000639111.2:c.632-32T= ENSP00000492125.2:n.632-32T=
ENST00000639213.2:c.632-32T= MANE Select ENSP00000491909.2:n.632-32T=
ENST00000639278.1:c.560-32T= ENSP00000491958.1:n.560-32T=
ENST00000639384.1:c.632-32T= ENSP00000491240.1:n.632-32T=
ENST00000639424.1:c.107+35751T= ENSP00000491245.1:n.107+35751T=
ENST00000639683.1:c.566-32T= ENSP00000492581.1:n.566-32T=
ENST00000639975.1:c.566-32T= ENSP00000492096.1:n.566-32T=
ENST00000640574.1:c.347-32T= ENSP00000491582.1:n.347-32T=
ENST00000640739.1:n.3131T=
ENST00000640910.1:c.70-32T=
ENST00000640985.1:c.545-32T= ENSP00000492293.1:n.545-32T=
ENST00000641017.1:c.632-32T= ENSP00000493461.1:n.632-32T=
ENST00000356592.7:c.632-32T= ENSP00000349000.3:n.632-32T=
ENST00000361925.8:c.632-32T= ENSP00000354651.4:n.632-32T=
ENST00000414552.6:c.752-32T= ENSP00000410732.2:n.752-32T=
ENST00000522053.1:c.347-32T= ENSP00000430182.1:n.347-32T=
ENST00000522990.5:c.*234-32T= ENSP00000430732.1:n.*234-32T=
ENST00000523372.1:c.753-32T= ENSP00000430124.1:n.753-32T=
NM_000816.3:c.632-32T= NP_000807.2:n.632-32T=
NM_198903.2:c.752-32T= NP_944493.2:n.752-32T=
NM_198904.2:c.632-32T= NP_944494.1:n.632-32T=
NM_001375339.1:c.623-32T= NP_001362268.1:n.623-32T=
NM_001375340.1:c.632-32T= NP_001362269.1:n.632-32T=
NM_001375341.1:c.632-32T= NP_001362270.1:n.632-32T=
NM_001375342.1:c.632-32T= NP_001362271.1:n.632-32T=
NM_001375343.1:c.752-32T= NP_001362272.1:n.752-32T=
NM_001375344.1:c.632-32T= NP_001362273.1:n.632-32T=
NM_001375345.1:c.566-32T= NP_001362274.1:n.566-32T=
NM_001375346.1:c.566-32T= NP_001362275.1:n.566-32T=
NM_001375347.1:c.545-32T= NP_001362276.1:n.545-32T=
NM_001375348.1:c.212-32T= NP_001362277.1:n.212-32T=
NM_001375349.1:c.347-32T= NP_001362278.1:n.347-32T=
NM_001375350.1:c.212-32T= NP_001362279.1:n.212-32T=
NM_198904.3:c.632-32T= NP_944494.1:n.632-32T=
NM_198904.4:c.632-32T= MANE Select NP_944494.1:n.632-32T=