Canonical Allele Identifier: CA10623930
Gene: GABRG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 352656
ClinVar RCV Id: RCV000284562
dbSNP Id: rs424740

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162154029T>A , CM000667.2:g.162154029T>A GRCh38
NC_000005.9:g.161581035T>A , CM000667.1:g.161581035T>A GRCh37
NC_000005.8:g.161513613T>A NCBI36
NG_009290.1:g.91388T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000356592.8:n.2090T>A
ENST00000361925.9:c.*661T>A ENSP00000354651.5:p.=
ENST00000638552.1:c.*661T>A ENSP00000491763.1:p.=
ENST00000638660.1:c.*661T>A ENSP00000492869.1:p.=
ENST00000638772.1:c.*4686T>A ENSP00000491557.1:p.=
ENST00000638877.1:n.1966T>A
ENST00000639046.1:c.*661T>A ENSP00000492659.1:p.=
ENST00000639111.2:c.*661T>A ENSP00000492125.2:p.=
ENST00000639213.2:c.*661T>A MANE Select ENSP00000491909.2:p.=
ENST00000639278.1:n.2752T>A ENSP00000491958.1:p.=
ENST00000639384.1:c.*2270T>A ENSP00000491240.1:p.=
ENST00000639424.1:c.*1289T>A ENSP00000491245.1:p.=
ENST00000639683.1:c.*661T>A ENSP00000492581.1:p.=
ENST00000639975.1:c.*661T>A ENSP00000492096.1:p.=
ENST00000640500.1:n.1363T>A
ENST00000640739.1:n.7036T>A
ENST00000640985.1:c.*661T>A ENSP00000492293.1:p.=
ENST00000641017.1:n.2158T>A ENSP00000493461.1:p.=
ENST00000356592.7:c.*661T>A ENSP00000349000.3:p.=
ENST00000414552.6:c.*661T>A ENSP00000410732.2:p.=
ENST00000522990.5:c.*1667T>A ENSP00000430732.1:p.=
NM_000816.3:c.*661T>A NP_000807.2:p.=
NM_198903.2:c.*661T>A NP_944493.2:p.=
NM_198904.2:c.*661T>A NP_944494.1:p.=
NM_001375339.1:c.*661T>A NP_001362268.1:p.=
NM_001375340.1:c.*923T>A NP_001362269.1:p.=
NM_001375341.1:c.*661T>A NP_001362270.1:p.=
NM_001375342.1:c.*661T>A NP_001362271.1:p.=
NM_001375343.1:c.*661T>A NP_001362272.1:p.=
NM_001375344.1:c.*661T>A NP_001362273.1:p.=
NM_001375345.1:c.*661T>A NP_001362274.1:p.=
NM_001375346.1:c.*661T>A NP_001362275.1:p.=
NM_001375347.1:c.*661T>A NP_001362276.1:p.=
NM_001375348.1:c.*661T>A NP_001362277.1:p.=
NM_001375349.1:c.*661T>A NP_001362278.1:p.=
NM_001375350.1:c.*661T>A NP_001362279.1:p.=
NM_198904.3:c.*661T>A NP_944494.1:p.=
NM_198904.4:c.*661T>A MANE Select NP_944494.1:p.=