Canonical Allele Identifier: CA2245821730
Gene: CHRNB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454099T= , CM000679.2:g.7454099T= GRCh38
NC_000017.10:g.7357418T= , CM000679.1:g.7357418T= GRCh37
NC_000017.9:g.7298142T= NCBI36
NG_008026.1:g.14013T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.821-198T= MANE Select ENSP00000304290.2:n.821-198T=
ENST00000306071.6:c.821-198T= ENSP00000304290.2:n.821-198T=
ENST00000536404.6:c.605-198T= ENSP00000439209.2:n.605-198T=
ENST00000570557.5:c.484-198T=
ENST00000573209.1:n.1765-198T=
ENST00000576360.1:c.605-345T= ENSP00000459092.1:n.605-345T=
NM_000747.2:c.821-198T= NP_000738.2:n.821-198T=
NM_000747.3:c.821-198T= MANE Select NP_000738.2:n.821-198T=