Canonical Allele Identifier: CA2245821911
Gene: CHRNB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454526A= , CM000679.2:g.7454526A= GRCh38
NC_000017.10:g.7357845A= , CM000679.1:g.7357845A= GRCh37
NC_000017.9:g.7298569A= NCBI36
NG_008026.1:g.14440A=

Transcript Alleles

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