Canonical Allele Identifier: CA362182346

Gene: GABRG2

Linked Data

• ClinVar Variation Id: 2663882
• ClinVar RCV Id: RCV003444148
• MyVariant Identifiers: chr5:g.161576138C>A (hg19) ; chr5:g.162149132C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162149132C>A , CM000667.2:g.162149132C>A	GRCh38
NC_000005.9:g.161576138C>A , CM000667.1:g.161576138C>A	GRCh37
NC_000005.8:g.161508716C>A	NCBI36
NG_009290.1:g.86491C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.948C>A
ENST00000361925.9:c.1067C>A	ENSP00000354651.5:p.Thr356Asn
ENST00000522053.2:n.838C>A
ENST00000523372.2:c.1030C>A
ENST00000638253.1:n.201C>A
ENST00000638552.1:c.662C>A	ENSP00000491763.1:p.Thr221Asn
ENST00000638660.1:c.662C>A	ENSP00000492869.1:p.Thr221Asn
ENST00000638772.1:c.947C>A	ENSP00000491557.1:p.Thr316Asn
ENST00000638877.1:c.824C>A
ENST00000639046.1:c.338C>A	ENSP00000492659.1:p.Thr113Asn
ENST00000639111.2:c.947C>A	ENSP00000492125.2:p.Thr316Asn
ENST00000639213.2:c.947C>A MANE Select	ENSP00000491909.2:p.Thr316Asn
ENST00000639278.1:c.875C>A	ENSP00000491958.1:p.Thr292Asn
ENST00000639384.1:c.947C>A	ENSP00000491240.1:p.Thr316Asn
ENST00000639424.1:c.*147C>A	ENSP00000491245.1:n.*147C>A
ENST00000639683.1:c.881C>A	ENSP00000492581.1:p.Thr294Asn
ENST00000639975.1:c.881C>A	ENSP00000492096.1:p.Thr294Asn
ENST00000640500.1:n.245C>A
ENST00000640574.1:c.662C>A	ENSP00000491582.1:p.Thr221Asn
ENST00000640739.1:n.3478C>A
ENST00000640910.1:c.385C>A
ENST00000640985.1:c.860C>A	ENSP00000492293.1:p.Thr287Asn
ENST00000641017.1:c.947C>A	ENSP00000493461.1:p.Thr316Asn
ENST00000356592.7:c.947C>A	ENSP00000349000.3:p.Thr316Asn
ENST00000361925.8:c.947C>A	ENSP00000354651.4:p.Thr316Asn
ENST00000414552.6:c.1067C>A	ENSP00000410732.2:p.Thr356Asn
ENST00000522053.1:c.662C>A	ENSP00000430182.1:p.Thr221Asn
ENST00000522990.5:c.*549C>A	ENSP00000430732.1:n.*549C>A
ENST00000523372.1:c.1068C>A	ENSP00000430124.1:n.1068C>A
NM_000816.3:c.947C>A	NP_000807.2:p.Thr316Asn
NM_198903.2:c.1067C>A	NP_944493.2:p.Thr356Asn
NM_198904.2:c.947C>A	NP_944494.1:p.Thr316Asn
NM_001375339.1:c.938C>A	NP_001362268.1:p.Thr313Asn
NM_001375340.1:c.923-2598C>A	NP_001362269.1:n.923-2598C>A
NM_001375341.1:c.944C>A	NP_001362270.1:p.Thr315Asn
NM_001375342.1:c.944C>A	NP_001362271.1:p.Thr315Asn
NM_001375343.1:c.1067C>A	NP_001362272.1:p.Thr356Asn
NM_001375344.1:c.986C>A	NP_001362273.1:p.Thr329Asn
NM_001375345.1:c.881C>A	NP_001362274.1:p.Thr294Asn
NM_001375346.1:c.881C>A	NP_001362275.1:p.Thr294Asn
NM_001375347.1:c.860C>A	NP_001362276.1:p.Thr287Asn
NM_001375348.1:c.527C>A	NP_001362277.1:p.Thr176Asn
NM_001375349.1:c.662C>A	NP_001362278.1:p.Thr221Asn
NM_001375350.1:c.527C>A	NP_001362279.1:p.Thr176Asn
NM_198904.3:c.947C>A	NP_944494.1:p.Thr316Asn
NM_198904.4:c.947C>A MANE Select	NP_944494.1:p.Thr316Asn