Canonical Allele Identifier: CA10623936

Gene: GABRG2

Linked Data

• ClinVar Variation Id: 352667
• ClinVar RCV Id: RCV000375622
• dbSNP Id: rs886060388
• MyVariant Identifiers: chr5:g.161582263C>A (hg19) ; chr5:g.162155257C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162155257C>A , CM000667.2:g.162155257C>A	GRCh38
NC_000005.9:g.161582263C>A , CM000667.1:g.161582263C>A	GRCh37
NC_000005.8:g.161514841C>A	NCBI36
NG_009290.1:g.92616C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000356592.8:c.3318C>A
ENST00000361925.9:c.*1889C>A	ENSP00000354651.5:n.*1889C>A
ENST00000638552.1:c.*1889C>A	ENSP00000491763.1:n.*1889C>A
ENST00000638660.1:c.*1889C>A	ENSP00000492869.1:n.*1889C>A
ENST00000638772.1:c.*5914C>A	ENSP00000491557.1:n.*5914C>A
ENST00000638877.1:c.3194C>A
ENST00000639046.1:c.*1889C>A	ENSP00000492659.1:n.*1889C>A
ENST00000639111.2:c.*1889C>A	ENSP00000492125.2:n.*1889C>A
ENST00000639213.2:c.*1889C>A MANE Select	ENSP00000491909.2:n.*1889C>A
ENST00000639384.1:c.*3498C>A	ENSP00000491240.1:n.*3498C>A
ENST00000639683.1:c.*1889C>A	ENSP00000492581.1:n.*1889C>A
ENST00000639975.1:c.*1889C>A	ENSP00000492096.1:n.*1889C>A
ENST00000640500.1:n.2591C>A
ENST00000640739.1:n.8264C>A
ENST00000641017.1:c.3386C>A	ENSP00000493461.1:n.3386C>A
ENST00000356592.7:c.*1889C>A	ENSP00000349000.3:n.*1889C>A
ENST00000414552.6:c.*1889C>A	ENSP00000410732.2:n.*1889C>A
NM_000816.3:c.*1889C>A	NP_000807.2:n.*1889C>A
NM_198903.2:c.*1889C>A	NP_944493.2:n.*1889C>A
NM_198904.2:c.*1889C>A	NP_944494.1:n.*1889C>A
NM_001375339.1:c.*1889C>A	NP_001362268.1:n.*1889C>A
NM_001375340.1:c.*2151C>A	NP_001362269.1:n.*2151C>A
NM_001375341.1:c.*1889C>A	NP_001362270.1:n.*1889C>A
NM_001375342.1:c.*1889C>A	NP_001362271.1:n.*1889C>A
NM_001375343.1:c.*1889C>A	NP_001362272.1:n.*1889C>A
NM_001375344.1:c.*1889C>A	NP_001362273.1:n.*1889C>A
NM_001375345.1:c.*1889C>A	NP_001362274.1:n.*1889C>A
NM_001375346.1:c.*1889C>A	NP_001362275.1:n.*1889C>A
NM_001375347.1:c.*1889C>A	NP_001362276.1:n.*1889C>A
NM_001375348.1:c.*1889C>A	NP_001362277.1:n.*1889C>A
NM_001375349.1:c.*1889C>A	NP_001362278.1:n.*1889C>A
NM_001375350.1:c.*1889C>A	NP_001362279.1:n.*1889C>A
NM_198904.3:c.*1889C>A	NP_944494.1:n.*1889C>A
NM_198904.4:c.*1889C>A MANE Select	NP_944494.1:n.*1889C>A