Canonical Allele Identifier: CA362183608

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161580218T>A (hg19) ; chr5:g.162153212T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153212T>A , CM000667.2:g.162153212T>A	GRCh38
NC_000005.9:g.161580218T>A , CM000667.1:g.161580218T>A	GRCh37
NC_000005.8:g.161512796T>A	NCBI36
NG_009290.1:g.90571T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1273T>A
ENST00000361925.9:c.1368T>A	ENSP00000354651.5:p.Ser456Arg
ENST00000523372.2:c.1331T>A
ENST00000638253.1:n.526T>A
ENST00000638552.1:c.963T>A	ENSP00000491763.1:p.Ser321Arg
ENST00000638660.1:c.987T>A	ENSP00000492869.1:p.Ser329Arg
ENST00000638772.1:c.*3869T>A	ENSP00000491557.1:n.*3869T>A
ENST00000638877.1:c.1149T>A
ENST00000639046.1:c.639T>A	ENSP00000492659.1:p.Ser213Arg
ENST00000639111.2:c.1248T>A	ENSP00000492125.2:p.Ser416Arg
ENST00000639213.2:c.1272T>A MANE Select	ENSP00000491909.2:p.Ser424Arg
ENST00000639278.1:c.1935T>A	ENSP00000491958.1:n.1935T>A
ENST00000639384.1:c.*1453T>A	ENSP00000491240.1:n.*1453T>A
ENST00000639424.1:c.*472T>A	ENSP00000491245.1:n.*472T>A
ENST00000639683.1:c.1206T>A	ENSP00000492581.1:p.Ser402Arg
ENST00000639975.1:c.1182T>A	ENSP00000492096.1:p.Ser394Arg
ENST00000640500.1:n.546T>A
ENST00000640739.1:n.6219T>A
ENST00000640910.1:c.710T>A
ENST00000640985.1:c.1185T>A	ENSP00000492293.1:p.Ser395Arg
ENST00000641017.1:c.1341T>A	ENSP00000493461.1:p.Ser447Arg
ENST00000356592.7:c.1272T>A	ENSP00000349000.3:p.Ser424Arg
ENST00000361925.8:c.1248T>A	ENSP00000354651.4:p.Ser416Arg
ENST00000414552.6:c.1392T>A	ENSP00000410732.2:p.Ser464Arg
ENST00000522990.5:c.*850T>A	ENSP00000430732.1:n.*850T>A
ENST00000523372.1:c.1369T>A	ENSP00000430124.1:n.1369T>A
NM_000816.3:c.1248T>A	NP_000807.2:p.Ser416Arg
NM_198903.2:c.1392T>A	NP_944493.2:p.Ser464Arg
NM_198904.2:c.1272T>A	NP_944494.1:p.Ser424Arg
NM_001375339.1:c.1263T>A	NP_001362268.1:p.Ser421Arg
NM_001375340.1:c.*106T>A	NP_001362269.1:n.*106T>A
NM_001375341.1:c.1269T>A	NP_001362270.1:p.Ser423Arg
NM_001375342.1:c.1245T>A	NP_001362271.1:p.Ser415Arg
NM_001375343.1:c.1368T>A	NP_001362272.1:p.Ser456Arg
NM_001375344.1:c.1311T>A	NP_001362273.1:p.Ser437Arg
NM_001375345.1:c.1182T>A	NP_001362274.1:p.Ser394Arg
NM_001375346.1:c.1206T>A	NP_001362275.1:p.Ser402Arg
NM_001375347.1:c.1185T>A	NP_001362276.1:p.Ser395Arg
NM_001375348.1:c.828T>A	NP_001362277.1:p.Ser276Arg
NM_001375349.1:c.963T>A	NP_001362278.1:p.Ser321Arg
NM_001375350.1:c.852T>A	NP_001362279.1:p.Ser284Arg
NM_198904.3:c.1272T>A	NP_944494.1:p.Ser424Arg
NM_198904.4:c.1272T>A MANE Select	NP_944494.1:p.Ser424Arg