Canonical Allele Identifier: CA362182305

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161576119A>T (hg19) ; chr5:g.162149113A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162149113A>T , CM000667.2:g.162149113A>T	GRCh38
NC_000005.9:g.161576119A>T , CM000667.1:g.161576119A>T	GRCh37
NC_000005.8:g.161508697A>T	NCBI36
NG_009290.1:g.86472A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.929A>T
ENST00000361925.9:c.1048A>T	ENSP00000354651.5:p.Thr350Ser
ENST00000522053.2:n.819A>T
ENST00000523372.2:c.1011A>T
ENST00000638253.1:n.182A>T
ENST00000638552.1:c.643A>T	ENSP00000491763.1:p.Thr215Ser
ENST00000638660.1:c.643A>T	ENSP00000492869.1:p.Thr215Ser
ENST00000638772.1:c.928A>T	ENSP00000491557.1:p.Thr310Ser
ENST00000638877.1:c.805A>T
ENST00000639046.1:c.319A>T	ENSP00000492659.1:p.Thr107Ser
ENST00000639111.2:c.928A>T	ENSP00000492125.2:p.Thr310Ser
ENST00000639213.2:c.928A>T MANE Select	ENSP00000491909.2:p.Thr310Ser
ENST00000639278.1:c.856A>T	ENSP00000491958.1:p.Thr286Ser
ENST00000639384.1:c.928A>T	ENSP00000491240.1:p.Thr310Ser
ENST00000639424.1:c.*128A>T	ENSP00000491245.1:n.*128A>T
ENST00000639683.1:c.862A>T	ENSP00000492581.1:p.Thr288Ser
ENST00000639975.1:c.862A>T	ENSP00000492096.1:p.Thr288Ser
ENST00000640500.1:n.226A>T
ENST00000640574.1:c.643A>T	ENSP00000491582.1:p.Thr215Ser
ENST00000640739.1:n.3459A>T
ENST00000640910.1:c.366A>T
ENST00000640985.1:c.841A>T	ENSP00000492293.1:p.Thr281Ser
ENST00000641017.1:c.928A>T	ENSP00000493461.1:p.Thr310Ser
ENST00000356592.7:c.928A>T	ENSP00000349000.3:p.Thr310Ser
ENST00000361925.8:c.928A>T	ENSP00000354651.4:p.Thr310Ser
ENST00000414552.6:c.1048A>T	ENSP00000410732.2:p.Thr350Ser
ENST00000522053.1:c.643A>T	ENSP00000430182.1:p.Thr215Ser
ENST00000522990.5:c.*530A>T	ENSP00000430732.1:n.*530A>T
ENST00000523372.1:c.1049A>T	ENSP00000430124.1:n.1049A>T
NM_000816.3:c.928A>T	NP_000807.2:p.Thr310Ser
NM_198903.2:c.1048A>T	NP_944493.2:p.Thr350Ser
NM_198904.2:c.928A>T	NP_944494.1:p.Thr310Ser
NM_001375339.1:c.919A>T	NP_001362268.1:p.Thr307Ser
NM_001375340.1:c.923-2617A>T	NP_001362269.1:n.923-2617A>T
NM_001375341.1:c.925A>T	NP_001362270.1:p.Thr309Ser
NM_001375342.1:c.925A>T	NP_001362271.1:p.Thr309Ser
NM_001375343.1:c.1048A>T	NP_001362272.1:p.Thr350Ser
NM_001375344.1:c.967A>T	NP_001362273.1:p.Thr323Ser
NM_001375345.1:c.862A>T	NP_001362274.1:p.Thr288Ser
NM_001375346.1:c.862A>T	NP_001362275.1:p.Thr288Ser
NM_001375347.1:c.841A>T	NP_001362276.1:p.Thr281Ser
NM_001375348.1:c.508A>T	NP_001362277.1:p.Thr170Ser
NM_001375349.1:c.643A>T	NP_001362278.1:p.Thr215Ser
NM_001375350.1:c.508A>T	NP_001362279.1:p.Thr170Ser
NM_198904.3:c.928A>T	NP_944494.1:p.Thr310Ser
NM_198904.4:c.928A>T MANE Select	NP_944494.1:p.Thr310Ser