Canonical Allele Identifier: CA447610299

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161576229C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162149223C>T , CM000667.2:g.162149223C>T	GRCh38
NC_000005.9:g.161576229C>T , CM000667.1:g.161576229C>T	GRCh37
NC_000005.8:g.161508807C>T	NCBI36
NG_009290.1:g.86582C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356592.8:c.1039C>T
ENST00000361925.9:c.1158C>T	ENSP00000354651.5:p.Val386=
ENST00000523372.2:c.1121C>T
ENST00000638253.1:n.292C>T
ENST00000638552.1:c.753C>T	ENSP00000491763.1:p.Val251=
ENST00000638660.1:c.753C>T	ENSP00000492869.1:p.Val251=
ENST00000638772.1:c.1038C>T	ENSP00000491557.1:p.Val346=
ENST00000638877.1:c.915C>T
ENST00000639046.1:c.429C>T	ENSP00000492659.1:p.Val143=
ENST00000639111.2:c.1038C>T	ENSP00000492125.2:p.Val346=
ENST00000639213.2:c.1038C>T MANE Select	ENSP00000491909.2:p.Val346=
ENST00000639278.1:c.966C>T	ENSP00000491958.1:p.Val322=
ENST00000639384.1:c.1038C>T	ENSP00000491240.1:p.Val346=
ENST00000639424.1:c.*238C>T	ENSP00000491245.1:n.*238C>T
ENST00000639683.1:c.972C>T	ENSP00000492581.1:p.Val324=
ENST00000639975.1:c.972C>T	ENSP00000492096.1:p.Val324=
ENST00000640500.1:n.336C>T
ENST00000640574.1:c.753C>T	ENSP00000491582.1:p.Val251=
ENST00000640739.1:n.3569C>T
ENST00000640910.1:c.476C>T
ENST00000640985.1:c.951C>T	ENSP00000492293.1:p.Val317=
ENST00000641017.1:c.1038C>T	ENSP00000493461.1:p.Val346=
ENST00000356592.7:c.1038C>T	ENSP00000349000.3:p.Val346=
ENST00000361925.8:c.1038C>T	ENSP00000354651.4:p.Val346=
ENST00000414552.6:c.1158C>T	ENSP00000410732.2:p.Val386=
ENST00000522990.5:c.*640C>T	ENSP00000430732.1:n.*640C>T
ENST00000523372.1:c.1159C>T	ENSP00000430124.1:n.1159C>T
NM_000816.3:c.1038C>T	NP_000807.2:p.Val346=
NM_198903.2:c.1158C>T	NP_944493.2:p.Val386=
NM_198904.2:c.1038C>T	NP_944494.1:p.Val346=
NM_001375339.1:c.1029C>T	NP_001362268.1:p.Val343=
NM_001375340.1:c.923-2507C>T	NP_001362269.1:n.923-2507C>T
NM_001375341.1:c.1035C>T	NP_001362270.1:p.Val345=
NM_001375342.1:c.1035C>T	NP_001362271.1:p.Val345=
NM_001375343.1:c.1158C>T	NP_001362272.1:p.Val386=
NM_001375344.1:c.1077C>T	NP_001362273.1:p.Val359=
NM_001375345.1:c.972C>T	NP_001362274.1:p.Val324=
NM_001375346.1:c.972C>T	NP_001362275.1:p.Val324=
NM_001375347.1:c.951C>T	NP_001362276.1:p.Val317=
NM_001375348.1:c.618C>T	NP_001362277.1:p.Val206=
NM_001375349.1:c.753C>T	NP_001362278.1:p.Val251=
NM_001375350.1:c.618C>T	NP_001362279.1:p.Val206=
NM_198904.3:c.1038C>T	NP_944494.1:p.Val346=
NM_198904.4:c.1038C>T MANE Select	NP_944494.1:p.Val346=