Canonical Allele Identifier: CA2245821886
Gene: CHRNB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454468A= , CM000679.2:g.7454468A= GRCh38
NC_000017.10:g.7357787A= , CM000679.1:g.7357787A= GRCh37
NC_000017.9:g.7298511A= NCBI36
NG_008026.1:g.14382A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.992A= MANE Select ENSP00000304290.2:p.Asn331=
ENST00000306071.6:c.992A= ENSP00000304290.2:p.Asn331=
ENST00000536404.6:c.776A= ENSP00000439209.2:p.Asn259=
ENST00000570557.5:c.655A=
ENST00000573209.1:n.1936A=
ENST00000576360.1:c.629A= ENSP00000459092.1:p.Asn210=
NM_000747.2:c.992A= NP_000738.2:p.Asn331=
NM_000747.3:c.992A= MANE Select NP_000738.2:p.Asn331=