Canonical Allele Identifier: CA362185165
Gene: GABRG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162103979C>A , CM000667.2:g.162103979C>A GRCh38
NC_000005.9:g.161530985C>A , CM000667.1:g.161530985C>A GRCh37
NC_000005.8:g.161463563C>A NCBI36
NG_009290.1:g.41338C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.684C>A
ENST00000361925.9:c.842C>A ENSP00000354651.5:p.Ser281Ter
ENST00000522053.2:n.613C>A
ENST00000523372.2:c.805C>A
ENST00000638552.1:c.437C>A ENSP00000491763.1:p.Ser146Ter
ENST00000638660.1:c.437C>A ENSP00000492869.1:p.Ser146Ter
ENST00000638772.1:c.722C>A ENSP00000491557.1:p.Ser241Ter
ENST00000638782.1:n.784C>A
ENST00000638877.1:c.599C>A
ENST00000639046.1:c.113C>A ENSP00000492659.1:p.Ser38Ter
ENST00000639111.2:c.722C>A ENSP00000492125.2:p.Ser241Ter
ENST00000639213.2:c.722C>A MANE Select ENSP00000491909.2:p.Ser241Ter
ENST00000639278.1:c.650C>A ENSP00000491958.1:p.Ser217Ter
ENST00000639384.1:c.722C>A ENSP00000491240.1:p.Ser241Ter
ENST00000639424.1:c.107+35873C>A ENSP00000491245.1:n.107+35873C>A
ENST00000639683.1:c.656C>A ENSP00000492581.1:p.Ser219Ter
ENST00000639975.1:c.656C>A ENSP00000492096.1:p.Ser219Ter
ENST00000640574.1:c.437C>A ENSP00000491582.1:p.Ser146Ter
ENST00000640739.1:n.3253C>A
ENST00000640910.1:c.160C>A
ENST00000640985.1:c.635C>A ENSP00000492293.1:p.Ser212Ter
ENST00000641017.1:c.722C>A ENSP00000493461.1:p.Ser241Ter
ENST00000356592.7:c.722C>A ENSP00000349000.3:p.Ser241Ter
ENST00000361925.8:c.722C>A ENSP00000354651.4:p.Ser241Ter
ENST00000414552.6:c.842C>A ENSP00000410732.2:p.Ser281Ter
ENST00000522053.1:c.437C>A ENSP00000430182.1:p.Ser146Ter
ENST00000522990.5:c.*324C>A ENSP00000430732.1:n.*324C>A
ENST00000523372.1:c.843C>A ENSP00000430124.1:n.843C>A
NM_000816.3:c.722C>A NP_000807.2:p.Ser241Ter
NM_198903.2:c.842C>A NP_944493.2:p.Ser281Ter
NM_198904.2:c.722C>A NP_944494.1:p.Ser241Ter
NM_001375339.1:c.713C>A NP_001362268.1:p.Ser238Ter
NM_001375340.1:c.722C>A NP_001362269.1:p.Ser241Ter
NM_001375341.1:c.722C>A NP_001362270.1:p.Ser241Ter
NM_001375342.1:c.722C>A NP_001362271.1:p.Ser241Ter
NM_001375343.1:c.842C>A NP_001362272.1:p.Ser281Ter
NM_001375344.1:c.722C>A NP_001362273.1:p.Ser241Ter
NM_001375345.1:c.656C>A NP_001362274.1:p.Ser219Ter
NM_001375346.1:c.656C>A NP_001362275.1:p.Ser219Ter
NM_001375347.1:c.635C>A NP_001362276.1:p.Ser212Ter
NM_001375348.1:c.302C>A NP_001362277.1:p.Ser101Ter
NM_001375349.1:c.437C>A NP_001362278.1:p.Ser146Ter
NM_001375350.1:c.302C>A NP_001362279.1:p.Ser101Ter
NM_198904.3:c.722C>A NP_944494.1:p.Ser241Ter
NM_198904.4:c.722C>A MANE Select NP_944494.1:p.Ser241Ter