Canonical Allele Identifier: CA2245821926
Gene: CHRNB1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454549A= , CM000679.2:g.7454549A= GRCh38
NC_000017.10:g.7357868A= , CM000679.1:g.7357868A= GRCh37
NC_000017.9:g.7298592A= NCBI36
NG_008026.1:g.14463A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1044+29A= MANE Select ENSP00000304290.2:n.1044+29A=
ENST00000306071.6:c.1044+29A= ENSP00000304290.2:n.1044+29A=
ENST00000536404.6:c.828+29A= ENSP00000439209.2:n.828+29A=
ENST00000570557.5:c.707+29A=
ENST00000573209.1:n.1988+29A=
ENST00000576360.1:c.681+29A= ENSP00000459092.1:n.681+29A=
NM_000747.2:c.1044+29A= NP_000738.2:n.1044+29A=
NM_000747.3:c.1044+29A= MANE Select NP_000738.2:n.1044+29A=
Search 100 bp 5'
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