Canonical Allele Identifier: CA397802639
Gene: CHRNB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7455886T>A , CM000679.2:g.7455886T>A GRCh38
NC_000017.10:g.7359205T>A , CM000679.1:g.7359205T>A GRCh37
NC_000017.9:g.7299929T>A NCBI36
NG_008026.1:g.15800T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1310T>A MANE Select ENSP00000304290.2:p.Val437Asp
ENST00000306071.6:c.1310T>A ENSP00000304290.2:p.Val437Asp
ENST00000536404.6:c.1094T>A ENSP00000439209.2:p.Val365Asp
ENST00000575379.1:c.-83T>A ENSP00000461751.1:n.-83T>A
ENST00000576360.1:c.947T>A ENSP00000459092.1:p.Val316Asp
NM_000747.2:c.1310T>A NP_000738.2:p.Val437Asp
NM_000747.3:c.1310T>A MANE Select NP_000738.2:p.Val437Asp