Canonical Allele Identifier: CA2590159126
Gene: CHRNB1 HGNC NCBI

Linked Data

dbSNP Id: rs2150842234

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454054del , CM000679.2:g.7454054del GRCh38
NC_000017.10:g.7357373del , CM000679.1:g.7357373del GRCh37
NC_000017.9:g.7298097del NCBI36
NG_008026.1:g.13968del

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.821-243del MANE Select ENSP00000304290.2:n.821-243del
ENST00000306071.6:c.821-243del ENSP00000304290.2:n.821-243del
ENST00000536404.6:c.605-243del ENSP00000439209.2:n.605-243del
ENST00000570557.5:c.484-243del
ENST00000573209.1:n.1765-243del
ENST00000576360.1:c.605-390del ENSP00000459092.1:n.605-390del
NM_000747.2:c.821-243del NP_000738.2:n.821-243del
NM_000747.3:c.821-243del MANE Select NP_000738.2:n.821-243del