Canonical Allele Identifier: CA447692044

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161580362C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153356C>T , CM000667.2:g.162153356C>T	GRCh38
NC_000005.9:g.161580362C>T , CM000667.1:g.161580362C>T	GRCh37
NC_000005.8:g.161512940C>T	NCBI36
NG_009290.1:g.90715C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1417C>T
ENST00000361925.9:c.1512C>T	ENSP00000354651.5:p.Tyr504=
ENST00000523372.2:c.1475C>T
ENST00000638253.1:n.670C>T
ENST00000638552.1:c.1107C>T	ENSP00000491763.1:p.Tyr369=
ENST00000638660.1:c.1131C>T	ENSP00000492869.1:p.Tyr377=
ENST00000638772.1:c.*4013C>T	ENSP00000491557.1:n.*4013C>T
ENST00000638877.1:c.1293C>T
ENST00000639046.1:c.783C>T	ENSP00000492659.1:p.Tyr261=
ENST00000639111.2:c.1392C>T	ENSP00000492125.2:p.Tyr464=
ENST00000639213.2:c.1416C>T MANE Select	ENSP00000491909.2:p.Tyr472=
ENST00000639278.1:c.2079C>T	ENSP00000491958.1:n.2079C>T
ENST00000639384.1:c.*1597C>T	ENSP00000491240.1:n.*1597C>T
ENST00000639424.1:c.*616C>T	ENSP00000491245.1:n.*616C>T
ENST00000639683.1:c.1350C>T	ENSP00000492581.1:p.Tyr450=
ENST00000639975.1:c.1326C>T	ENSP00000492096.1:p.Tyr442=
ENST00000640500.1:n.690C>T
ENST00000640739.1:n.6363C>T
ENST00000640910.1:c.854C>T
ENST00000640985.1:c.1329C>T	ENSP00000492293.1:p.Tyr443=
ENST00000641017.1:c.1485C>T	ENSP00000493461.1:p.Tyr495=
ENST00000356592.7:c.1416C>T	ENSP00000349000.3:p.Tyr472=
ENST00000361925.8:c.1392C>T	ENSP00000354651.4:p.Tyr464=
ENST00000414552.6:c.1536C>T	ENSP00000410732.2:p.Tyr512=
ENST00000522990.5:c.*994C>T	ENSP00000430732.1:n.*994C>T
ENST00000523372.1:c.1513C>T	ENSP00000430124.1:n.1513C>T
NM_000816.3:c.1392C>T	NP_000807.2:p.Tyr464=
NM_198903.2:c.1536C>T	NP_944493.2:p.Tyr512=
NM_198904.2:c.1416C>T	NP_944494.1:p.Tyr472=
NM_001375339.1:c.1407C>T	NP_001362268.1:p.Tyr469=
NM_001375340.1:c.*250C>T	NP_001362269.1:n.*250C>T
NM_001375341.1:c.1413C>T	NP_001362270.1:p.Tyr471=
NM_001375342.1:c.1389C>T	NP_001362271.1:p.Tyr463=
NM_001375343.1:c.1512C>T	NP_001362272.1:p.Tyr504=
NM_001375344.1:c.1455C>T	NP_001362273.1:p.Tyr485=
NM_001375345.1:c.1326C>T	NP_001362274.1:p.Tyr442=
NM_001375346.1:c.1350C>T	NP_001362275.1:p.Tyr450=
NM_001375347.1:c.1329C>T	NP_001362276.1:p.Tyr443=
NM_001375348.1:c.972C>T	NP_001362277.1:p.Tyr324=
NM_001375349.1:c.1107C>T	NP_001362278.1:p.Tyr369=
NM_001375350.1:c.996C>T	NP_001362279.1:p.Tyr332=
NM_198904.3:c.1416C>T	NP_944494.1:p.Tyr472=
NM_198904.4:c.1416C>T MANE Select	NP_944494.1:p.Tyr472=