Canonical Allele Identifier: CA2245822530
Gene: CHRNB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7455779T= , CM000679.2:g.7455779T= GRCh38
NC_000017.10:g.7359098T= , CM000679.1:g.7359098T= GRCh37
NC_000017.9:g.7299822T= NCBI36
NG_008026.1:g.15693T=

Transcript Alleles

HGVS Amino-acid change
ENST00000306071.7:c.1218-15T= MANE Select ENSP00000304290.2:n.1218-15T=
ENST00000306071.6:c.1218-15T= ENSP00000304290.2:n.1218-15T=
ENST00000536404.6:c.1002-15T= ENSP00000439209.2:n.1002-15T=
ENST00000570557.5:c.881-15T=
ENST00000575379.1:c.-190T= ENSP00000461751.1:n.-190T=
ENST00000576360.1:c.855-15T= ENSP00000459092.1:n.855-15T=
NM_000747.2:c.1218-15T= NP_000738.2:n.1218-15T=
NM_000747.3:c.1218-15T= MANE Select NP_000738.2:n.1218-15T=