Canonical Allele Identifier: CA2245821742
Gene: CHRNB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454130A= , CM000679.2:g.7454130A= GRCh38
NC_000017.10:g.7357449A= , CM000679.1:g.7357449A= GRCh37
NC_000017.9:g.7298173A= NCBI36
NG_008026.1:g.14044A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.821-167A= MANE Select ENSP00000304290.2:n.821-167A=
ENST00000306071.6:c.821-167A= ENSP00000304290.2:n.821-167A=
ENST00000536404.6:c.605-167A= ENSP00000439209.2:n.605-167A=
ENST00000570557.5:c.484-167A=
ENST00000573209.1:n.1765-167A=
ENST00000576360.1:c.605-314A= ENSP00000459092.1:n.605-314A=
NM_000747.2:c.821-167A= NP_000738.2:n.821-167A=
NM_000747.3:c.821-167A= MANE Select NP_000738.2:n.821-167A=