Canonical Allele Identifier: CA447610335

Gene: GABRG2

Linked Data

• gnomAD v4: 5-162149272-C-A
• COSMIC: COSM3613593
• MyVariant Identifiers: chr5:g.161576278C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162149272C>A , CM000667.2:g.162149272C>A	GRCh38
NC_000005.9:g.161576278C>A , CM000667.1:g.161576278C>A	GRCh37
NC_000005.8:g.161508856C>A	NCBI36
NG_009290.1:g.86631C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1088C>A
ENST00000361925.9:c.1207C>A	ENSP00000354651.5:p.Arg403=
ENST00000523372.2:c.1170C>A
ENST00000638253.1:n.341C>A
ENST00000638552.1:c.802C>A	ENSP00000491763.1:p.Arg268=
ENST00000638660.1:c.802C>A	ENSP00000492869.1:p.Arg268=
ENST00000638772.1:c.1087C>A	ENSP00000491557.1:p.Arg363=
ENST00000638877.1:c.964C>A
ENST00000639046.1:c.478C>A	ENSP00000492659.1:p.Arg160=
ENST00000639111.2:c.1087C>A	ENSP00000492125.2:p.Arg363=
ENST00000639213.2:c.1087C>A MANE Select	ENSP00000491909.2:p.Arg363=
ENST00000639278.1:c.1015C>A	ENSP00000491958.1:p.Arg339=
ENST00000639384.1:c.1087C>A	ENSP00000491240.1:p.Arg363=
ENST00000639424.1:c.*287C>A	ENSP00000491245.1:n.*287C>A
ENST00000639683.1:c.1021C>A	ENSP00000492581.1:p.Arg341=
ENST00000639975.1:c.1021C>A	ENSP00000492096.1:p.Arg341=
ENST00000640500.1:n.385C>A
ENST00000640574.1:c.802C>A	ENSP00000491582.1:p.Arg268=
ENST00000640739.1:n.3618C>A
ENST00000640910.1:c.525C>A
ENST00000640985.1:c.1000C>A	ENSP00000492293.1:p.Arg334=
ENST00000641017.1:c.1087C>A	ENSP00000493461.1:p.Arg363=
ENST00000356592.7:c.1087C>A	ENSP00000349000.3:p.Arg363=
ENST00000361925.8:c.1087C>A	ENSP00000354651.4:p.Arg363=
ENST00000414552.6:c.1207C>A	ENSP00000410732.2:p.Arg403=
ENST00000522990.5:c.*689C>A	ENSP00000430732.1:n.*689C>A
ENST00000523372.1:c.1208C>A	ENSP00000430124.1:n.1208C>A
NM_000816.3:c.1087C>A	NP_000807.2:p.Arg363=
NM_198903.2:c.1207C>A	NP_944493.2:p.Arg403=
NM_198904.2:c.1087C>A	NP_944494.1:p.Arg363=
NM_001375339.1:c.1078C>A	NP_001362268.1:p.Arg360=
NM_001375340.1:c.923-2458C>A	NP_001362269.1:n.923-2458C>A
NM_001375341.1:c.1084C>A	NP_001362270.1:p.Arg362=
NM_001375342.1:c.1084C>A	NP_001362271.1:p.Arg362=
NM_001375343.1:c.1207C>A	NP_001362272.1:p.Arg403=
NM_001375344.1:c.1126C>A	NP_001362273.1:p.Arg376=
NM_001375345.1:c.1021C>A	NP_001362274.1:p.Arg341=
NM_001375346.1:c.1021C>A	NP_001362275.1:p.Arg341=
NM_001375347.1:c.1000C>A	NP_001362276.1:p.Arg334=
NM_001375348.1:c.667C>A	NP_001362277.1:p.Arg223=
NM_001375349.1:c.802C>A	NP_001362278.1:p.Arg268=
NM_001375350.1:c.667C>A	NP_001362279.1:p.Arg223=
NM_198904.3:c.1087C>A	NP_944494.1:p.Arg363=
NM_198904.4:c.1087C>A MANE Select	NP_944494.1:p.Arg363=