Canonical Allele Identifier: CA2189590129
Gene: CHRNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78601901G= , CM000677.2:g.78601901G= GRCh38
NC_000015.9:g.78894243G= , CM000677.1:g.78894243G= GRCh37
NC_000015.8:g.76681298G= NCBI36
NG_016143.1:g.24395C=

Transcript Alleles

HGVS Amino-acid change
ENST00000326828.6:c.741C= MANE Select ENSP00000315602.5:p.Asn247=
ENST00000326828.5:c.741C= ENSP00000315602.5:p.Asn247=
ENST00000348639.7:c.741C= ENSP00000267951.4:p.Asn247=
ENST00000558903.1:n.448C=
ENST00000559658.5:c.741C= ENSP00000452896.1:p.Asn247=
NM_000743.4:c.741C= NP_000734.2:p.Asn247=
NM_001166694.1:c.741C= NP_001160166.1:p.Asn247=
NR_046313.1:n.1242C=
XM_006720382.1:c.540C= XP_006720445.1:p.Asn180=
XM_011521173.1:c.660C= XP_011519475.1:p.Asn220=
XM_006720382.3:c.540C= XP_006720445.1:p.Asn180=
NM_000743.5:c.741C= MANE Select NP_000734.2:p.Asn247=
NM_001166694.2:c.741C= NP_001160166.1:p.Asn247=
NR_046313.2:n.943C=