Canonical Allele Identifier: CA2245822539
Gene: CHRNB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7455791C= , CM000679.2:g.7455791C= GRCh38
NC_000017.10:g.7359110C= , CM000679.1:g.7359110C= GRCh37
NC_000017.9:g.7299834C= NCBI36
NG_008026.1:g.15705C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1218-3C= MANE Select ENSP00000304290.2:n.1218-3C=
ENST00000306071.6:c.1218-3C= ENSP00000304290.2:n.1218-3C=
ENST00000536404.6:c.1002-3C= ENSP00000439209.2:n.1002-3C=
ENST00000570557.5:c.881-3C=
ENST00000575379.1:c.-178C= ENSP00000461751.1:n.-178C=
ENST00000576360.1:c.855-3C= ENSP00000459092.1:n.855-3C=
NM_000747.2:c.1218-3C= NP_000738.2:n.1218-3C=
NM_000747.3:c.1218-3C= MANE Select NP_000738.2:n.1218-3C=