Canonical Allele Identifier: CA342631193
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2855881
ClinVar RCV Id: RCV003746093

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571783C>A , CM000663.2:g.154571783C>A GRCh38
NC_000001.10:g.154544259C>A , CM000663.1:g.154544259C>A GRCh37
NC_000001.9:g.152810883C>A NCBI36
NG_008027.1:g.9003C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.960C>A MANE Select ENSP00000357461.3:p.Asn320Lys
ENST00000636034.1:c.960C>A ENSP00000489703.1:p.Asn320Lys
ENST00000637900.1:c.966C>A ENSP00000490474.1:p.Asn322Lys
ENST00000368476.3:c.960C>A ENSP00000357461.3:p.Asn320Lys
NM_000748.2:c.960C>A NP_000739.1:p.Asn320Lys
XM_017000180.2:c.450C>A XP_016855669.1:p.Asn150Lys
XR_001736952.2:n.1212C>A
NM_000748.3:c.960C>A MANE Select NP_000739.1:p.Asn320Lys