Canonical Allele Identifier: CA362183938

Gene: GABRG2

Linked Data

• dbSNP Id: rs1765505931
• MyVariant Identifiers: chr5:g.161580298C>T (hg19) ; chr5:g.162153292C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153292C>T , CM000667.2:g.162153292C>T	GRCh38
NC_000005.9:g.161580298C>T , CM000667.1:g.161580298C>T	GRCh37
NC_000005.8:g.161512876C>T	NCBI36
NG_009290.1:g.90651C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1353C>T
ENST00000361925.9:c.1448C>T	ENSP00000354651.5:p.Ser483Phe
ENST00000523372.2:c.1411C>T
ENST00000638253.1:n.606C>T
ENST00000638552.1:c.1043C>T	ENSP00000491763.1:p.Ser348Phe
ENST00000638660.1:c.1067C>T	ENSP00000492869.1:p.Ser356Phe
ENST00000638772.1:c.*3949C>T	ENSP00000491557.1:n.*3949C>T
ENST00000638877.1:c.1229C>T
ENST00000639046.1:c.719C>T	ENSP00000492659.1:p.Ser240Phe
ENST00000639111.2:c.1328C>T	ENSP00000492125.2:p.Ser443Phe
ENST00000639213.2:c.1352C>T MANE Select	ENSP00000491909.2:p.Ser451Phe
ENST00000639278.1:c.2015C>T	ENSP00000491958.1:n.2015C>T
ENST00000639384.1:c.*1533C>T	ENSP00000491240.1:n.*1533C>T
ENST00000639424.1:c.*552C>T	ENSP00000491245.1:n.*552C>T
ENST00000639683.1:c.1286C>T	ENSP00000492581.1:p.Ser429Phe
ENST00000639975.1:c.1262C>T	ENSP00000492096.1:p.Ser421Phe
ENST00000640500.1:n.626C>T
ENST00000640739.1:n.6299C>T
ENST00000640910.1:c.790C>T
ENST00000640985.1:c.1265C>T	ENSP00000492293.1:p.Ser422Phe
ENST00000641017.1:c.1421C>T	ENSP00000493461.1:p.Ser474Phe
ENST00000356592.7:c.1352C>T	ENSP00000349000.3:p.Ser451Phe
ENST00000361925.8:c.1328C>T	ENSP00000354651.4:p.Ser443Phe
ENST00000414552.6:c.1472C>T	ENSP00000410732.2:p.Ser491Phe
ENST00000522990.5:c.*930C>T	ENSP00000430732.1:n.*930C>T
ENST00000523372.1:c.1449C>T	ENSP00000430124.1:n.1449C>T
NM_000816.3:c.1328C>T	NP_000807.2:p.Ser443Phe
NM_198903.2:c.1472C>T	NP_944493.2:p.Ser491Phe
NM_198904.2:c.1352C>T	NP_944494.1:p.Ser451Phe
NM_001375339.1:c.1343C>T	NP_001362268.1:p.Ser448Phe
NM_001375340.1:c.*186C>T	NP_001362269.1:n.*186C>T
NM_001375341.1:c.1349C>T	NP_001362270.1:p.Ser450Phe
NM_001375342.1:c.1325C>T	NP_001362271.1:p.Ser442Phe
NM_001375343.1:c.1448C>T	NP_001362272.1:p.Ser483Phe
NM_001375344.1:c.1391C>T	NP_001362273.1:p.Ser464Phe
NM_001375345.1:c.1262C>T	NP_001362274.1:p.Ser421Phe
NM_001375346.1:c.1286C>T	NP_001362275.1:p.Ser429Phe
NM_001375347.1:c.1265C>T	NP_001362276.1:p.Ser422Phe
NM_001375348.1:c.908C>T	NP_001362277.1:p.Ser303Phe
NM_001375349.1:c.1043C>T	NP_001362278.1:p.Ser348Phe
NM_001375350.1:c.932C>T	NP_001362279.1:p.Ser311Phe
NM_198904.3:c.1352C>T	NP_944494.1:p.Ser451Phe
NM_198904.4:c.1352C>T MANE Select	NP_944494.1:p.Ser451Phe