Canonical Allele Identifier: CA2245821960
Gene: CHRNB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454643G= , CM000679.2:g.7454643G= GRCh38
NC_000017.10:g.7357962G= , CM000679.1:g.7357962G= GRCh37
NC_000017.9:g.7298686G= NCBI36
NG_008026.1:g.14557G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1044+123G= MANE Select ENSP00000304290.2:n.1044+123G=
ENST00000306071.6:c.1044+123G= ENSP00000304290.2:n.1044+123G=
ENST00000536404.6:c.828+123G= ENSP00000439209.2:n.828+123G=
ENST00000570557.5:c.707+123G=
ENST00000573209.1:n.1988+123G=
ENST00000576360.1:c.681+123G= ENSP00000459092.1:n.681+123G=
NM_000747.2:c.1044+123G= NP_000738.2:n.1044+123G=
NM_000747.3:c.1044+123G= MANE Select NP_000738.2:n.1044+123G=