Canonical Allele Identifier: CA2245821919
Gene: CHRNB1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454541C= , CM000679.2:g.7454541C= GRCh38
NC_000017.10:g.7357860C= , CM000679.1:g.7357860C= GRCh37
NC_000017.9:g.7298584C= NCBI36
NG_008026.1:g.14455C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1044+21C= MANE Select ENSP00000304290.2:n.1044+21C=
ENST00000306071.6:c.1044+21C= ENSP00000304290.2:n.1044+21C=
ENST00000536404.6:c.828+21C= ENSP00000439209.2:n.828+21C=
ENST00000570557.5:c.707+21C=
ENST00000573209.1:n.1988+21C=
ENST00000576360.1:c.681+21C= ENSP00000459092.1:n.681+21C=
NM_000747.2:c.1044+21C= NP_000738.2:n.1044+21C=
NM_000747.3:c.1044+21C= MANE Select NP_000738.2:n.1044+21C=
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