Canonical Allele Identifier: CA2635846695
Gene: CHRNB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7455760del , CM000679.2:g.7455760del GRCh38
NC_000017.10:g.7359079del , CM000679.1:g.7359079del GRCh37
NC_000017.9:g.7299803del NCBI36
NG_008026.1:g.15674del

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1218-34del MANE Select ENSP00000304290.2:n.1218-34del
ENST00000306071.6:c.1218-34del ENSP00000304290.2:n.1218-34del
ENST00000536404.6:c.1002-34del ENSP00000439209.2:n.1002-34del
ENST00000570557.5:c.881-34del
ENST00000575379.1:c.-209del ENSP00000461751.1:n.-209del
ENST00000576360.1:c.855-34del ENSP00000459092.1:n.855-34del
NM_000747.2:c.1218-34del NP_000738.2:n.1218-34del
NM_000747.3:c.1218-34del MANE Select NP_000738.2:n.1218-34del