Canonical Allele Identifier: CA362182436

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161576182T>G (hg19) ; chr5:g.162149176T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162149176T>G , CM000667.2:g.162149176T>G	GRCh38
NC_000005.9:g.161576182T>G , CM000667.1:g.161576182T>G	GRCh37
NC_000005.8:g.161508760T>G	NCBI36
NG_009290.1:g.86535T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.992T>G
ENST00000361925.9:c.1111T>G	ENSP00000354651.5:p.Tyr371Asp
ENST00000523372.2:c.1074T>G
ENST00000638253.1:n.245T>G
ENST00000638552.1:c.706T>G	ENSP00000491763.1:p.Tyr236Asp
ENST00000638660.1:c.706T>G	ENSP00000492869.1:p.Tyr236Asp
ENST00000638772.1:c.991T>G	ENSP00000491557.1:p.Tyr331Asp
ENST00000638877.1:c.868T>G
ENST00000639046.1:c.382T>G	ENSP00000492659.1:p.Tyr128Asp
ENST00000639111.2:c.991T>G	ENSP00000492125.2:p.Tyr331Asp
ENST00000639213.2:c.991T>G MANE Select	ENSP00000491909.2:p.Tyr331Asp
ENST00000639278.1:c.919T>G	ENSP00000491958.1:p.Tyr307Asp
ENST00000639384.1:c.991T>G	ENSP00000491240.1:p.Tyr331Asp
ENST00000639424.1:c.*191T>G	ENSP00000491245.1:n.*191T>G
ENST00000639683.1:c.925T>G	ENSP00000492581.1:p.Tyr309Asp
ENST00000639975.1:c.925T>G	ENSP00000492096.1:p.Tyr309Asp
ENST00000640500.1:n.289T>G
ENST00000640574.1:c.706T>G	ENSP00000491582.1:p.Tyr236Asp
ENST00000640739.1:n.3522T>G
ENST00000640910.1:c.429T>G
ENST00000640985.1:c.904T>G	ENSP00000492293.1:p.Tyr302Asp
ENST00000641017.1:c.991T>G	ENSP00000493461.1:p.Tyr331Asp
ENST00000356592.7:c.991T>G	ENSP00000349000.3:p.Tyr331Asp
ENST00000361925.8:c.991T>G	ENSP00000354651.4:p.Tyr331Asp
ENST00000414552.6:c.1111T>G	ENSP00000410732.2:p.Tyr371Asp
ENST00000522990.5:c.*593T>G	ENSP00000430732.1:n.*593T>G
ENST00000523372.1:c.1112T>G	ENSP00000430124.1:n.1112T>G
NM_000816.3:c.991T>G	NP_000807.2:p.Tyr331Asp
NM_198903.2:c.1111T>G	NP_944493.2:p.Tyr371Asp
NM_198904.2:c.991T>G	NP_944494.1:p.Tyr331Asp
NM_001375339.1:c.982T>G	NP_001362268.1:p.Tyr328Asp
NM_001375340.1:c.923-2554T>G	NP_001362269.1:n.923-2554T>G
NM_001375341.1:c.988T>G	NP_001362270.1:p.Tyr330Asp
NM_001375342.1:c.988T>G	NP_001362271.1:p.Tyr330Asp
NM_001375343.1:c.1111T>G	NP_001362272.1:p.Tyr371Asp
NM_001375344.1:c.1030T>G	NP_001362273.1:p.Tyr344Asp
NM_001375345.1:c.925T>G	NP_001362274.1:p.Tyr309Asp
NM_001375346.1:c.925T>G	NP_001362275.1:p.Tyr309Asp
NM_001375347.1:c.904T>G	NP_001362276.1:p.Tyr302Asp
NM_001375348.1:c.571T>G	NP_001362277.1:p.Tyr191Asp
NM_001375349.1:c.706T>G	NP_001362278.1:p.Tyr236Asp
NM_001375350.1:c.571T>G	NP_001362279.1:p.Tyr191Asp
NM_198904.3:c.991T>G	NP_944494.1:p.Tyr331Asp
NM_198904.4:c.991T>G MANE Select	NP_944494.1:p.Tyr331Asp