Canonical Allele Identifier: CA30834647
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1037431
ClinVar RCV Id: RCV001340577
dbSNP Id: rs868235334

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571716G>A , CM000663.2:g.154571716G>A GRCh38
NC_000001.10:g.154544192G>A , CM000663.1:g.154544192G>A GRCh37
NC_000001.9:g.152810816G>A NCBI36
NG_008027.1:g.8936G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.893G>A MANE Select ENSP00000357461.3:p.Gly298Asp
ENST00000636034.1:c.893G>A ENSP00000489703.1:p.Gly298Asp
ENST00000637900.1:c.899G>A ENSP00000490474.1:p.Gly300Asp
ENST00000368476.3:c.893G>A ENSP00000357461.3:p.Gly298Asp
NM_000748.2:c.893G>A NP_000739.1:p.Gly298Asp
XM_017000180.2:c.383G>A XP_016855669.1:p.Gly128Asp
XR_001736952.2:n.1145G>A
NM_000748.3:c.893G>A MANE Select NP_000739.1:p.Gly298Asp