Canonical Allele Identifier: CA439245933
Gene: GABRB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2811982
ClinVar RCV Id: RCV003685176
dbSNP Id: rs748346475
gnomAD v3: 4-47406926-G-A
gnomAD v4: 4-47406926-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.47406926G>A , CM000666.2:g.47406926G>A GRCh38
NC_000004.11:g.47408943G>A , CM000666.1:g.47408943G>A GRCh37
NC_000004.10:g.47103700G>A NCBI36
NG_051831.1:g.380649G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295454.8:c.1080G>A MANE Select ENSP00000295454.3:p.Gln360=
ENST00000295454.7:c.1080G>A ENSP00000295454.3:p.Gln360=
NM_000812.3:c.1080G>A NP_000803.2:p.Gln360=
XM_011513678.1:c.1059G>A XP_011511980.1:p.Gln353=
XM_017007985.1:c.429G>A XP_016863474.1:p.Gln143=
XM_024453976.1:c.981G>A XP_024309744.1:p.Gln327=
XM_024453977.1:c.981G>A XP_024309745.1:p.Gln327=
XM_024453978.1:c.981G>A XP_024309746.1:p.Gln327=
NM_000812.4:c.1080G>A MANE Select NP_000803.2:p.Gln360=