Canonical Allele Identifier: CA447691963

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161580299C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153293C>G , CM000667.2:g.162153293C>G	GRCh38
NC_000005.9:g.161580299C>G , CM000667.1:g.161580299C>G	GRCh37
NC_000005.8:g.161512877C>G	NCBI36
NG_009290.1:g.90652C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1354C>G
ENST00000361925.9:c.1449C>G	ENSP00000354651.5:p.Ser483=
ENST00000523372.2:c.1412C>G
ENST00000638253.1:n.607C>G
ENST00000638552.1:c.1044C>G	ENSP00000491763.1:p.Ser348=
ENST00000638660.1:c.1068C>G	ENSP00000492869.1:p.Ser356=
ENST00000638772.1:c.*3950C>G	ENSP00000491557.1:n.*3950C>G
ENST00000638877.1:c.1230C>G
ENST00000639046.1:c.720C>G	ENSP00000492659.1:p.Ser240=
ENST00000639111.2:c.1329C>G	ENSP00000492125.2:p.Ser443=
ENST00000639213.2:c.1353C>G MANE Select	ENSP00000491909.2:p.Ser451=
ENST00000639278.1:c.2016C>G	ENSP00000491958.1:n.2016C>G
ENST00000639384.1:c.*1534C>G	ENSP00000491240.1:n.*1534C>G
ENST00000639424.1:c.*553C>G	ENSP00000491245.1:n.*553C>G
ENST00000639683.1:c.1287C>G	ENSP00000492581.1:p.Ser429=
ENST00000639975.1:c.1263C>G	ENSP00000492096.1:p.Ser421=
ENST00000640500.1:n.627C>G
ENST00000640739.1:n.6300C>G
ENST00000640910.1:c.791C>G
ENST00000640985.1:c.1266C>G	ENSP00000492293.1:p.Ser422=
ENST00000641017.1:c.1422C>G	ENSP00000493461.1:p.Ser474=
ENST00000356592.7:c.1353C>G	ENSP00000349000.3:p.Ser451=
ENST00000361925.8:c.1329C>G	ENSP00000354651.4:p.Ser443=
ENST00000414552.6:c.1473C>G	ENSP00000410732.2:p.Ser491=
ENST00000522990.5:c.*931C>G	ENSP00000430732.1:n.*931C>G
ENST00000523372.1:c.1450C>G	ENSP00000430124.1:n.1450C>G
NM_000816.3:c.1329C>G	NP_000807.2:p.Ser443=
NM_198903.2:c.1473C>G	NP_944493.2:p.Ser491=
NM_198904.2:c.1353C>G	NP_944494.1:p.Ser451=
NM_001375339.1:c.1344C>G	NP_001362268.1:p.Ser448=
NM_001375340.1:c.*187C>G	NP_001362269.1:n.*187C>G
NM_001375341.1:c.1350C>G	NP_001362270.1:p.Ser450=
NM_001375342.1:c.1326C>G	NP_001362271.1:p.Ser442=
NM_001375343.1:c.1449C>G	NP_001362272.1:p.Ser483=
NM_001375344.1:c.1392C>G	NP_001362273.1:p.Ser464=
NM_001375345.1:c.1263C>G	NP_001362274.1:p.Ser421=
NM_001375346.1:c.1287C>G	NP_001362275.1:p.Ser429=
NM_001375347.1:c.1266C>G	NP_001362276.1:p.Ser422=
NM_001375348.1:c.909C>G	NP_001362277.1:p.Ser303=
NM_001375349.1:c.1044C>G	NP_001362278.1:p.Ser348=
NM_001375350.1:c.933C>G	NP_001362279.1:p.Ser311=
NM_198904.3:c.1353C>G	NP_944494.1:p.Ser451=
NM_198904.4:c.1353C>G MANE Select	NP_944494.1:p.Ser451=