Canonical Allele Identifier: CA1596356705
Gene: GABRG2 HGNC NCBI

Linked Data

dbSNP Id: rs183294

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162071731T>G , CM000667.2:g.162071731T>G GRCh38
NC_000005.9:g.161498737T>G , CM000667.1:g.161498737T>G GRCh37
NC_000005.8:g.161431315T>G NCBI36
NG_009290.1:g.9090T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000356592.8:c.69+3625T>G
ENST00000361925.9:c.107+3625T>G ENSP00000354651.5:n.107+3625T>G
ENST00000523372.2:c.69+3625T>G
ENST00000638552.1:c.-179+9822T>G ENSP00000491763.1:n.-179+9822T>G
ENST00000638660.1:c.-179+9822T>G ENSP00000492869.1:n.-179+9822T>G
ENST00000638772.1:c.107+3625T>G ENSP00000491557.1:n.107+3625T>G
ENST00000638782.1:n.169+3625T>G
ENST00000638877.1:c.46+3625T>G
ENST00000639046.1:c.23-32158T>G ENSP00000492659.1:n.23-32158T>G
ENST00000639111.2:c.107+3625T>G ENSP00000492125.2:n.107+3625T>G
ENST00000639213.2:c.107+3625T>G MANE Select ENSP00000491909.2:n.107+3625T>G
ENST00000639278.1:c.35+3625T>G ENSP00000491958.1:n.35+3625T>G
ENST00000639384.1:c.107+3625T>G ENSP00000491240.1:n.107+3625T>G
ENST00000639424.1:c.107+3625T>G ENSP00000491245.1:n.107+3625T>G
ENST00000639549.1:n.331+3625T>G
ENST00000639554.1:n.67+3625T>G
ENST00000639683.1:c.41+3625T>G ENSP00000492581.1:n.41+3625T>G
ENST00000639975.1:c.41+3625T>G ENSP00000492096.1:n.41+3625T>G
ENST00000640574.1:c.-179+9822T>G ENSP00000491582.1:n.-179+9822T>G
ENST00000640739.1:n.67+3625T>G
ENST00000640757.1:c.114-22097T>G ENSP00000492329.1:n.114-22097T>G
ENST00000640910.1:c.69+3625T>G
ENST00000640985.1:c.20+4090T>G ENSP00000492293.1:n.20+4090T>G
ENST00000641017.1:c.107+3625T>G ENSP00000493461.1:n.107+3625T>G
ENST00000356592.7:c.107+3625T>G ENSP00000349000.3:n.107+3625T>G
ENST00000361925.8:c.107+3625T>G ENSP00000354651.4:n.107+3625T>G
ENST00000414552.6:c.107+3625T>G ENSP00000410732.2:n.107+3625T>G
ENST00000522990.5:c.107+3625T>G ENSP00000430732.1:n.107+3625T>G
ENST00000523372.1:c.107+3625T>G ENSP00000430124.1:n.107+3625T>G
NM_000816.3:c.107+3625T>G NP_000807.2:n.107+3625T>G
NM_198903.2:c.107+3625T>G NP_944493.2:n.107+3625T>G
NM_198904.2:c.107+3625T>G NP_944494.1:n.107+3625T>G
NM_001375339.1:c.107+3625T>G NP_001362268.1:n.107+3625T>G
NM_001375340.1:c.107+3625T>G NP_001362269.1:n.107+3625T>G
NM_001375341.1:c.107+3625T>G NP_001362270.1:n.107+3625T>G
NM_001375342.1:c.107+3625T>G NP_001362271.1:n.107+3625T>G
NM_001375343.1:c.107+3625T>G NP_001362272.1:n.107+3625T>G
NM_001375344.1:c.107+3625T>G NP_001362273.1:n.107+3625T>G
NM_001375345.1:c.41+3625T>G NP_001362274.1:n.41+3625T>G
NM_001375346.1:c.41+3625T>G NP_001362275.1:n.41+3625T>G
NM_001375347.1:c.20+4090T>G NP_001362276.1:n.20+4090T>G
NM_001375348.1:c.-252+3625T>G NP_001362277.1:n.-252+3625T>G
NM_001375349.1:c.-300+3625T>G NP_001362278.1:n.-300+3625T>G
NM_001375350.1:c.-252+3625T>G NP_001362279.1:n.-252+3625T>G
NM_198904.3:c.107+3625T>G NP_944494.1:n.107+3625T>G
NM_198904.4:c.107+3625T>G MANE Select NP_944494.1:n.107+3625T>G