Canonical Allele Identifier: CA2189581191
Gene: CHRNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78596072G= , CM000677.2:g.78596072G= GRCh38
NC_000015.9:g.78888414G= , CM000677.1:g.78888414G= GRCh37
NC_000015.8:g.76675469G= NCBI36
NG_016143.1:g.30224C=
NG_023328.1:g.35553G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326828.6:c.*532C= MANE Select ENSP00000315602.5:n.*532C=
ENST00000326828.5:c.*532C= ENSP00000315602.5:n.*532C=
ENST00000348639.7:c.1390-2881C= ENSP00000267951.4:n.1390-2881C=
ENST00000559002.5:n.193+468C=
ENST00000559658.5:c.*64+468C= ENSP00000452896.1:n.*64+468C=
NM_000743.4:c.*532C= NP_000734.2:n.*532C=
NM_001166694.1:c.1390-2881C= NP_001160166.1:n.1390-2881C=
NR_046313.1:n.2083+468C=
XM_006720382.1:c.*532C= XP_006720445.1:n.*532C=
XM_011521173.1:c.*532C= XP_011519475.1:n.*532C=
XM_006720382.3:c.*532C= XP_006720445.1:n.*532C=
NM_000743.5:c.*532C= MANE Select NP_000734.2:n.*532C=
NM_001166694.2:c.1390-2881C= NP_001160166.1:n.1390-2881C=
NR_046313.2:n.1784+468C=