Canonical Allele Identifier: CA362185242
Gene: GABRG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162104015A>C , CM000667.2:g.162104015A>C GRCh38
NC_000005.9:g.161531021A>C , CM000667.1:g.161531021A>C GRCh37
NC_000005.8:g.161463599A>C NCBI36
NG_009290.1:g.41374A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.720A>C
ENST00000361925.9:c.878A>C ENSP00000354651.5:p.Lys293Thr
ENST00000522053.2:n.649A>C
ENST00000523372.2:c.841A>C
ENST00000638552.1:c.473A>C ENSP00000491763.1:p.Lys158Thr
ENST00000638660.1:c.473A>C ENSP00000492869.1:p.Lys158Thr
ENST00000638772.1:c.758A>C ENSP00000491557.1:p.Lys253Thr
ENST00000638782.1:n.820A>C
ENST00000638877.1:c.635A>C
ENST00000639046.1:c.149A>C ENSP00000492659.1:p.Lys50Thr
ENST00000639111.2:c.758A>C ENSP00000492125.2:p.Lys253Thr
ENST00000639213.2:c.758A>C MANE Select ENSP00000491909.2:p.Lys253Thr
ENST00000639278.1:c.686A>C ENSP00000491958.1:p.Lys229Thr
ENST00000639384.1:c.758A>C ENSP00000491240.1:p.Lys253Thr
ENST00000639424.1:c.107+35909A>C ENSP00000491245.1:n.107+35909A>C
ENST00000639683.1:c.692A>C ENSP00000492581.1:p.Lys231Thr
ENST00000639975.1:c.692A>C ENSP00000492096.1:p.Lys231Thr
ENST00000640574.1:c.473A>C ENSP00000491582.1:p.Lys158Thr
ENST00000640739.1:n.3289A>C
ENST00000640910.1:c.196A>C
ENST00000640985.1:c.671A>C ENSP00000492293.1:p.Lys224Thr
ENST00000641017.1:c.758A>C ENSP00000493461.1:p.Lys253Thr
ENST00000356592.7:c.758A>C ENSP00000349000.3:p.Lys253Thr
ENST00000361925.8:c.758A>C ENSP00000354651.4:p.Lys253Thr
ENST00000414552.6:c.878A>C ENSP00000410732.2:p.Lys293Thr
ENST00000522053.1:c.473A>C ENSP00000430182.1:p.Lys158Thr
ENST00000522990.5:c.*360A>C ENSP00000430732.1:n.*360A>C
ENST00000523372.1:c.879A>C ENSP00000430124.1:n.879A>C
NM_000816.3:c.758A>C NP_000807.2:p.Lys253Thr
NM_198903.2:c.878A>C NP_944493.2:p.Lys293Thr
NM_198904.2:c.758A>C NP_944494.1:p.Lys253Thr
NM_001375339.1:c.749A>C NP_001362268.1:p.Lys250Thr
NM_001375340.1:c.758A>C NP_001362269.1:p.Lys253Thr
NM_001375341.1:c.758A>C NP_001362270.1:p.Lys253Thr
NM_001375342.1:c.758A>C NP_001362271.1:p.Lys253Thr
NM_001375343.1:c.878A>C NP_001362272.1:p.Lys293Thr
NM_001375344.1:c.758A>C NP_001362273.1:p.Lys253Thr
NM_001375345.1:c.692A>C NP_001362274.1:p.Lys231Thr
NM_001375346.1:c.692A>C NP_001362275.1:p.Lys231Thr
NM_001375347.1:c.671A>C NP_001362276.1:p.Lys224Thr
NM_001375348.1:c.338A>C NP_001362277.1:p.Lys113Thr
NM_001375349.1:c.473A>C NP_001362278.1:p.Lys158Thr
NM_001375350.1:c.338A>C NP_001362279.1:p.Lys113Thr
NM_198904.3:c.758A>C NP_944494.1:p.Lys253Thr
NM_198904.4:c.758A>C MANE Select NP_944494.1:p.Lys253Thr