Canonical Allele Identifier: CA342631099
Gene: CHRNB2 HGNC NCBI

Linked Data

dbSNP Id: rs1233101483

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571737T>A , CM000663.2:g.154571737T>A GRCh38
NC_000001.10:g.154544213T>A , CM000663.1:g.154544213T>A GRCh37
NC_000001.9:g.152810837T>A NCBI36
NG_008027.1:g.8957T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.914T>A MANE Select ENSP00000357461.3:p.Met305Lys
ENST00000636034.1:c.914T>A ENSP00000489703.1:p.Met305Lys
ENST00000637900.1:c.920T>A ENSP00000490474.1:p.Met307Lys
ENST00000368476.3:c.914T>A ENSP00000357461.3:p.Met305Lys
NM_000748.2:c.914T>A NP_000739.1:p.Met305Lys
XM_017000180.2:c.404T>A XP_016855669.1:p.Met135Lys
XR_001736952.2:n.1166T>A
NM_000748.3:c.914T>A MANE Select NP_000739.1:p.Met305Lys