Canonical Allele Identifier: CA10619921
Gene: GABRG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 352632
ClinVar RCV Id: RCV000381041
dbSNP Id: rs886060378

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162067821T>A , CM000667.2:g.162067821T>A GRCh38
NC_000005.9:g.161494827T>A , CM000667.1:g.161494827T>A GRCh37
NC_000005.8:g.161427405T>A NCBI36
NG_009290.1:g.5180T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000638552.1:c.-179+5912T>A ENSP00000491763.1:n.-179+5912T>A
ENST00000638660.1:c.-179+5912T>A ENSP00000492869.1:n.-179+5912T>A
ENST00000638772.1:c.-179T>A ENSP00000491557.1:n.-179T>A
ENST00000639046.1:c.23-36068T>A ENSP00000492659.1:n.23-36068T>A
ENST00000639111.2:c.-179T>A ENSP00000492125.2:n.-179T>A
ENST00000639213.2:c.-179T>A MANE Select ENSP00000491909.2:n.-179T>A
ENST00000639384.1:c.-179T>A ENSP00000491240.1:n.-179T>A
ENST00000639424.1:c.-179T>A ENSP00000491245.1:n.-179T>A
ENST00000639549.1:n.46T>A
ENST00000639683.1:c.-4+180T>A ENSP00000492581.1:n.-4+180T>A
ENST00000639975.1:c.-4+180T>A ENSP00000492096.1:n.-4+180T>A
ENST00000640574.1:c.-179+5912T>A ENSP00000491582.1:n.-179+5912T>A
ENST00000640757.1:c.114-26007T>A ENSP00000492329.1:n.114-26007T>A
ENST00000640985.1:c.20+180T>A ENSP00000492293.1:n.20+180T>A
ENST00000356592.7:c.-179T>A ENSP00000349000.3:n.-179T>A
ENST00000361925.8:c.-179T>A ENSP00000354651.4:n.-179T>A
ENST00000414552.6:c.-179T>A ENSP00000410732.2:n.-179T>A
NM_000816.3:c.-179T>A NP_000807.2:n.-179T>A
NM_198903.2:c.-179T>A NP_944493.2:n.-179T>A
NM_198904.2:c.-179T>A NP_944494.1:n.-179T>A
NM_001375339.1:c.-179T>A NP_001362268.1:n.-179T>A
NM_001375340.1:c.-179T>A NP_001362269.1:n.-179T>A
NM_001375341.1:c.-179T>A NP_001362270.1:n.-179T>A
NM_001375342.1:c.-179T>A NP_001362271.1:n.-179T>A
NM_001375343.1:c.-179T>A NP_001362272.1:n.-179T>A
NM_001375344.1:c.-179T>A NP_001362273.1:n.-179T>A
NM_001375345.1:c.-4+180T>A NP_001362274.1:n.-4+180T>A
NM_001375346.1:c.-4+180T>A NP_001362275.1:n.-4+180T>A
NM_001375347.1:c.20+180T>A NP_001362276.1:n.20+180T>A
NM_001375348.1:c.-537T>A NP_001362277.1:n.-537T>A
NM_001375349.1:c.-585T>A NP_001362278.1:n.-585T>A
NM_001375350.1:c.-537T>A NP_001362279.1:n.-537T>A
NM_198904.3:c.-179T>A NP_944494.1:n.-179T>A
NM_198904.4:c.-179T>A MANE Select NP_944494.1:n.-179T>A