Canonical Allele Identifier: CA362182470

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161576197G>T (hg19) ; chr5:g.162149191G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162149191G>T , CM000667.2:g.162149191G>T	GRCh38
NC_000005.9:g.161576197G>T , CM000667.1:g.161576197G>T	GRCh37
NC_000005.8:g.161508775G>T	NCBI36
NG_009290.1:g.86550G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1007G>T
ENST00000361925.9:c.1126G>T	ENSP00000354651.5:p.Asp376Tyr
ENST00000523372.2:c.1089G>T
ENST00000638253.1:n.260G>T
ENST00000638552.1:c.721G>T	ENSP00000491763.1:p.Asp241Tyr
ENST00000638660.1:c.721G>T	ENSP00000492869.1:p.Asp241Tyr
ENST00000638772.1:c.1006G>T	ENSP00000491557.1:p.Asp336Tyr
ENST00000638877.1:c.883G>T
ENST00000639046.1:c.397G>T	ENSP00000492659.1:p.Asp133Tyr
ENST00000639111.2:c.1006G>T	ENSP00000492125.2:p.Asp336Tyr
ENST00000639213.2:c.1006G>T MANE Select	ENSP00000491909.2:p.Asp336Tyr
ENST00000639278.1:c.934G>T	ENSP00000491958.1:p.Asp312Tyr
ENST00000639384.1:c.1006G>T	ENSP00000491240.1:p.Asp336Tyr
ENST00000639424.1:c.*206G>T	ENSP00000491245.1:n.*206G>T
ENST00000639683.1:c.940G>T	ENSP00000492581.1:p.Asp314Tyr
ENST00000639975.1:c.940G>T	ENSP00000492096.1:p.Asp314Tyr
ENST00000640500.1:n.304G>T
ENST00000640574.1:c.721G>T	ENSP00000491582.1:p.Asp241Tyr
ENST00000640739.1:n.3537G>T
ENST00000640910.1:c.444G>T
ENST00000640985.1:c.919G>T	ENSP00000492293.1:p.Asp307Tyr
ENST00000641017.1:c.1006G>T	ENSP00000493461.1:p.Asp336Tyr
ENST00000356592.7:c.1006G>T	ENSP00000349000.3:p.Asp336Tyr
ENST00000361925.8:c.1006G>T	ENSP00000354651.4:p.Asp336Tyr
ENST00000414552.6:c.1126G>T	ENSP00000410732.2:p.Asp376Tyr
ENST00000522990.5:c.*608G>T	ENSP00000430732.1:n.*608G>T
ENST00000523372.1:c.1127G>T	ENSP00000430124.1:n.1127G>T
NM_000816.3:c.1006G>T	NP_000807.2:p.Asp336Tyr
NM_198903.2:c.1126G>T	NP_944493.2:p.Asp376Tyr
NM_198904.2:c.1006G>T	NP_944494.1:p.Asp336Tyr
NM_001375339.1:c.997G>T	NP_001362268.1:p.Asp333Tyr
NM_001375340.1:c.923-2539G>T	NP_001362269.1:n.923-2539G>T
NM_001375341.1:c.1003G>T	NP_001362270.1:p.Asp335Tyr
NM_001375342.1:c.1003G>T	NP_001362271.1:p.Asp335Tyr
NM_001375343.1:c.1126G>T	NP_001362272.1:p.Asp376Tyr
NM_001375344.1:c.1045G>T	NP_001362273.1:p.Asp349Tyr
NM_001375345.1:c.940G>T	NP_001362274.1:p.Asp314Tyr
NM_001375346.1:c.940G>T	NP_001362275.1:p.Asp314Tyr
NM_001375347.1:c.919G>T	NP_001362276.1:p.Asp307Tyr
NM_001375348.1:c.586G>T	NP_001362277.1:p.Asp196Tyr
NM_001375349.1:c.721G>T	NP_001362278.1:p.Asp241Tyr
NM_001375350.1:c.586G>T	NP_001362279.1:p.Asp196Tyr
NM_198904.3:c.1006G>T	NP_944494.1:p.Asp336Tyr
NM_198904.4:c.1006G>T MANE Select	NP_944494.1:p.Asp336Tyr