Canonical Allele Identifier: CA314744
Gene: GABRG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 205553
dbSNP Id: rs796052512

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162149297A>C , CM000667.2:g.162149297A>C GRCh38
NC_000005.9:g.161576303A>C , CM000667.1:g.161576303A>C GRCh37
NC_000005.8:g.161508881A>C NCBI36
NG_009290.1:g.86656A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000356592.8:c.1113A>C
ENST00000361925.9:c.1232A>C ENSP00000354651.5:p.Lys411Thr
ENST00000523372.2:c.1195A>C
ENST00000638253.1:n.366A>C
ENST00000638552.1:c.827A>C ENSP00000491763.1:p.Lys276Thr
ENST00000638660.1:c.827A>C ENSP00000492869.1:p.Lys276Thr
ENST00000638772.1:c.1112A>C ENSP00000491557.1:p.Lys371Thr
ENST00000638877.1:c.989A>C
ENST00000639046.1:c.503A>C ENSP00000492659.1:p.Lys168Thr
ENST00000639111.2:c.1112A>C ENSP00000492125.2:p.Lys371Thr
ENST00000639213.2:c.1112A>C MANE Select ENSP00000491909.2:p.Lys371Thr
ENST00000639278.1:c.1040A>C ENSP00000491958.1:p.Lys347Thr
ENST00000639384.1:c.1112A>C ENSP00000491240.1:p.Lys371Thr
ENST00000639424.1:c.*312A>C ENSP00000491245.1:n.*312A>C
ENST00000639683.1:c.1046A>C ENSP00000492581.1:p.Lys349Thr
ENST00000639975.1:c.1046A>C ENSP00000492096.1:p.Lys349Thr
ENST00000640500.1:n.410A>C
ENST00000640574.1:c.827A>C ENSP00000491582.1:p.Lys276Thr
ENST00000640739.1:n.3643A>C
ENST00000640910.1:c.550A>C
ENST00000640985.1:c.1025A>C ENSP00000492293.1:p.Lys342Thr
ENST00000641017.1:c.1112A>C ENSP00000493461.1:p.Lys371Thr
ENST00000356592.7:c.1112A>C ENSP00000349000.3:p.Lys371Thr
ENST00000361925.8:c.1112A>C ENSP00000354651.4:p.Lys371Thr
ENST00000414552.6:c.1232A>C ENSP00000410732.2:p.Lys411Thr
ENST00000522990.5:c.*714A>C ENSP00000430732.1:n.*714A>C
ENST00000523372.1:c.1233A>C ENSP00000430124.1:n.1233A>C
NM_000816.3:c.1112A>C NP_000807.2:p.Lys371Thr
NM_198903.2:c.1232A>C NP_944493.2:p.Lys411Thr
NM_198904.2:c.1112A>C NP_944494.1:p.Lys371Thr
NM_001375339.1:c.1103A>C NP_001362268.1:p.Lys368Thr
NM_001375340.1:c.923-2433A>C NP_001362269.1:n.923-2433A>C
NM_001375341.1:c.1109A>C NP_001362270.1:p.Lys370Thr
NM_001375342.1:c.1109A>C NP_001362271.1:p.Lys370Thr
NM_001375343.1:c.1232A>C NP_001362272.1:p.Lys411Thr
NM_001375344.1:c.1151A>C NP_001362273.1:p.Lys384Thr
NM_001375345.1:c.1046A>C NP_001362274.1:p.Lys349Thr
NM_001375346.1:c.1046A>C NP_001362275.1:p.Lys349Thr
NM_001375347.1:c.1025A>C NP_001362276.1:p.Lys342Thr
NM_001375348.1:c.692A>C NP_001362277.1:p.Lys231Thr
NM_001375349.1:c.827A>C NP_001362278.1:p.Lys276Thr
NM_001375350.1:c.692A>C NP_001362279.1:p.Lys231Thr
NM_198904.3:c.1112A>C NP_944494.1:p.Lys371Thr
NM_198904.4:c.1112A>C MANE Select NP_944494.1:p.Lys371Thr