Canonical Allele Identifier: CA2189590427
Gene: CHRNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78601993G= , CM000677.2:g.78601993G= GRCh38
NC_000015.9:g.78894335G= , CM000677.1:g.78894335G= GRCh37
NC_000015.8:g.76681390G= NCBI36
NG_016143.1:g.24303C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326828.6:c.649C= MANE Select ENSP00000315602.5:p.His217=
ENST00000326828.5:c.649C= ENSP00000315602.5:p.His217=
ENST00000348639.7:c.649C= ENSP00000267951.4:p.His217=
ENST00000558903.1:n.356C=
ENST00000559658.5:c.649C= ENSP00000452896.1:p.His217=
NM_000743.4:c.649C= NP_000734.2:p.His217=
NM_001166694.1:c.649C= NP_001160166.1:p.His217=
NR_046313.1:n.1150C=
XM_006720382.1:c.448C= XP_006720445.1:p.His150=
XM_011521173.1:c.568C= XP_011519475.1:p.His190=
XM_006720382.3:c.448C= XP_006720445.1:p.His150=
NM_000743.5:c.649C= MANE Select NP_000734.2:p.His217=
NM_001166694.2:c.649C= NP_001160166.1:p.His217=
NR_046313.2:n.851C=