Canonical Allele Identifier: CA3544868

Gene: GABRG2

Linked Data

• ClinVar Variation Id: 846848
• ClinVar RCV Id: RCV001050253
• dbSNP Id: rs149472714
• ExAC: 5:161576244 G / A
• gnomAD v2: 5-161576244-G-A
• gnomAD v3: 5-162149238-G-A
• gnomAD v4: 5-162149238-G-A
• MyVariant Identifiers: chr5:g.161576244G>A (hg19) ; chr5:g.162149238G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162149238G>A , CM000667.2:g.162149238G>A	GRCh38
NC_000005.9:g.161576244G>A , CM000667.1:g.161576244G>A	GRCh37
NC_000005.8:g.161508822G>A	NCBI36
NG_009290.1:g.86597G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1054G>A
ENST00000361925.9:c.1173G>A	ENSP00000354651.5:p.Val391=
ENST00000523372.2:c.1136G>A
ENST00000638253.1:n.307G>A
ENST00000638552.1:c.768G>A	ENSP00000491763.1:p.Val256=
ENST00000638660.1:c.768G>A	ENSP00000492869.1:p.Val256=
ENST00000638772.1:c.1053G>A	ENSP00000491557.1:p.Val351=
ENST00000638877.1:c.930G>A
ENST00000639046.1:c.444G>A	ENSP00000492659.1:p.Val148=
ENST00000639111.2:c.1053G>A	ENSP00000492125.2:p.Val351=
ENST00000639213.2:c.1053G>A MANE Select	ENSP00000491909.2:p.Val351=
ENST00000639278.1:c.981G>A	ENSP00000491958.1:p.Val327=
ENST00000639384.1:c.1053G>A	ENSP00000491240.1:p.Val351=
ENST00000639424.1:c.*253G>A	ENSP00000491245.1:n.*253G>A
ENST00000639683.1:c.987G>A	ENSP00000492581.1:p.Val329=
ENST00000639975.1:c.987G>A	ENSP00000492096.1:p.Val329=
ENST00000640500.1:n.351G>A
ENST00000640574.1:c.768G>A	ENSP00000491582.1:p.Val256=
ENST00000640739.1:n.3584G>A
ENST00000640910.1:c.491G>A
ENST00000640985.1:c.966G>A	ENSP00000492293.1:p.Val322=
ENST00000641017.1:c.1053G>A	ENSP00000493461.1:p.Val351=
ENST00000356592.7:c.1053G>A	ENSP00000349000.3:p.Val351=
ENST00000361925.8:c.1053G>A	ENSP00000354651.4:p.Val351=
ENST00000414552.6:c.1173G>A	ENSP00000410732.2:p.Val391=
ENST00000522990.5:c.*655G>A	ENSP00000430732.1:n.*655G>A
ENST00000523372.1:c.1174G>A	ENSP00000430124.1:n.1174G>A
NM_000816.3:c.1053G>A	NP_000807.2:p.Val351=
NM_198903.2:c.1173G>A	NP_944493.2:p.Val391=
NM_198904.2:c.1053G>A	NP_944494.1:p.Val351=
NM_001375339.1:c.1044G>A	NP_001362268.1:p.Val348=
NM_001375340.1:c.923-2492G>A	NP_001362269.1:n.923-2492G>A
NM_001375341.1:c.1050G>A	NP_001362270.1:p.Val350=
NM_001375342.1:c.1050G>A	NP_001362271.1:p.Val350=
NM_001375343.1:c.1173G>A	NP_001362272.1:p.Val391=
NM_001375344.1:c.1092G>A	NP_001362273.1:p.Val364=
NM_001375345.1:c.987G>A	NP_001362274.1:p.Val329=
NM_001375346.1:c.987G>A	NP_001362275.1:p.Val329=
NM_001375347.1:c.966G>A	NP_001362276.1:p.Val322=
NM_001375348.1:c.633G>A	NP_001362277.1:p.Val211=
NM_001375349.1:c.768G>A	NP_001362278.1:p.Val256=
NM_001375350.1:c.633G>A	NP_001362279.1:p.Val211=
NM_198904.3:c.1053G>A	NP_944494.1:p.Val351=
NM_198904.4:c.1053G>A MANE Select	NP_944494.1:p.Val351=