Canonical Allele Identifier: CA2245821748
Gene: CHRNB1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454133C= , CM000679.2:g.7454133C= GRCh38
NC_000017.10:g.7357452C= , CM000679.1:g.7357452C= GRCh37
NC_000017.9:g.7298176C= NCBI36
NG_008026.1:g.14047C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.821-164C= MANE Select ENSP00000304290.2:n.821-164C=
ENST00000306071.6:c.821-164C= ENSP00000304290.2:n.821-164C=
ENST00000536404.6:c.605-164C= ENSP00000439209.2:n.605-164C=
ENST00000570557.5:c.484-164C=
ENST00000573209.1:n.1765-164C=
ENST00000576360.1:c.605-311C= ENSP00000459092.1:n.605-311C=
NM_000747.2:c.821-164C= NP_000738.2:n.821-164C=
NM_000747.3:c.821-164C= MANE Select NP_000738.2:n.821-164C=
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