Canonical Allele Identifier: CA2245821906
Gene: CHRNB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454521G= , CM000679.2:g.7454521G= GRCh38
NC_000017.10:g.7357840G= , CM000679.1:g.7357840G= GRCh37
NC_000017.9:g.7298564G= NCBI36
NG_008026.1:g.14435G=

Transcript Alleles

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