Canonical Allele Identifier: CA362182059

Gene: GABRG2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162142216C>G , CM000667.2:g.162142216C>G	GRCh38
NC_000005.9:g.161569222C>G , CM000667.1:g.161569222C>G	GRCh37
NC_000005.8:g.161501800C>G	NCBI36
NG_009290.1:g.79575C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.823C>G
ENST00000361925.9:c.942C>G	ENSP00000354651.5:p.Tyr314Ter
ENST00000522053.2:n.713C>G
ENST00000523372.2:c.905C>G
ENST00000638253.1:n.76C>G
ENST00000638552.1:c.537C>G	ENSP00000491763.1:p.Tyr179Ter
ENST00000638660.1:c.537C>G	ENSP00000492869.1:p.Tyr179Ter
ENST00000638772.1:c.822C>G	ENSP00000491557.1:p.Tyr274Ter
ENST00000638782.1:n.884C>G
ENST00000638877.1:c.699C>G
ENST00000639046.1:c.213C>G	ENSP00000492659.1:p.Tyr71Ter
ENST00000639111.2:c.822C>G	ENSP00000492125.2:p.Tyr274Ter
ENST00000639213.2:c.822C>G MANE Select	ENSP00000491909.2:p.Tyr274Ter
ENST00000639278.1:c.750C>G	ENSP00000491958.1:p.Tyr250Ter
ENST00000639384.1:c.822C>G	ENSP00000491240.1:p.Tyr274Ter
ENST00000639424.1:c.*22C>G	ENSP00000491245.1:n.*22C>G
ENST00000639683.1:c.756C>G	ENSP00000492581.1:p.Tyr252Ter
ENST00000639975.1:c.756C>G	ENSP00000492096.1:p.Tyr252Ter
ENST00000640500.1:n.120C>G
ENST00000640574.1:c.537C>G	ENSP00000491582.1:p.Tyr179Ter
ENST00000640739.1:n.3353C>G
ENST00000640910.1:c.260C>G
ENST00000640985.1:c.735C>G	ENSP00000492293.1:p.Tyr245Ter
ENST00000641017.1:c.822C>G	ENSP00000493461.1:p.Tyr274Ter
ENST00000356592.7:c.822C>G	ENSP00000349000.3:p.Tyr274Ter
ENST00000361925.8:c.822C>G	ENSP00000354651.4:p.Tyr274Ter
ENST00000414552.6:c.942C>G	ENSP00000410732.2:p.Tyr314Ter
ENST00000522053.1:c.537C>G	ENSP00000430182.1:p.Tyr179Ter
ENST00000522990.5:c.*424C>G	ENSP00000430732.1:n.*424C>G
ENST00000523372.1:c.943C>G	ENSP00000430124.1:n.943C>G
NM_000816.3:c.822C>G	NP_000807.2:p.Tyr274Ter
NM_198903.2:c.942C>G	NP_944493.2:p.Tyr314Ter
NM_198904.2:c.822C>G	NP_944494.1:p.Tyr274Ter
NM_001375339.1:c.813C>G	NP_001362268.1:p.Tyr271Ter
NM_001375340.1:c.822C>G	NP_001362269.1:p.Tyr274Ter
NM_001375341.1:c.819C>G	NP_001362270.1:p.Tyr273Ter
NM_001375342.1:c.819C>G	NP_001362271.1:p.Tyr273Ter
NM_001375343.1:c.942C>G	NP_001362272.1:p.Tyr314Ter
NM_001375344.1:c.861C>G	NP_001362273.1:p.Tyr287Ter
NM_001375345.1:c.756C>G	NP_001362274.1:p.Tyr252Ter
NM_001375346.1:c.756C>G	NP_001362275.1:p.Tyr252Ter
NM_001375347.1:c.735C>G	NP_001362276.1:p.Tyr245Ter
NM_001375348.1:c.402C>G	NP_001362277.1:p.Tyr134Ter
NM_001375349.1:c.537C>G	NP_001362278.1:p.Tyr179Ter
NM_001375350.1:c.402C>G	NP_001362279.1:p.Tyr134Ter
NM_198904.3:c.822C>G	NP_944494.1:p.Tyr274Ter
NM_198904.4:c.822C>G MANE Select	NP_944494.1:p.Tyr274Ter