Canonical Allele Identifier: CA2245822529
Gene: CHRNB1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7455772T= , CM000679.2:g.7455772T= GRCh38
NC_000017.10:g.7359091T= , CM000679.1:g.7359091T= GRCh37
NC_000017.9:g.7299815T= NCBI36
NG_008026.1:g.15686T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1218-22T= MANE Select ENSP00000304290.2:n.1218-22T=
ENST00000306071.6:c.1218-22T= ENSP00000304290.2:n.1218-22T=
ENST00000536404.6:c.1002-22T= ENSP00000439209.2:n.1002-22T=
ENST00000570557.5:c.881-22T=
ENST00000575379.1:c.-197T= ENSP00000461751.1:n.-197T=
ENST00000576360.1:c.855-22T= ENSP00000459092.1:n.855-22T=
NM_000747.2:c.1218-22T= NP_000738.2:n.1218-22T=
NM_000747.3:c.1218-22T= MANE Select NP_000738.2:n.1218-22T=
Search 100 bp 5'
Search 100 bp 3'