Canonical Allele Identifier: CA2189590136
Gene: CHRNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78601907G= , CM000677.2:g.78601907G= GRCh38
NC_000015.9:g.78894249G= , CM000677.1:g.78894249G= GRCh37
NC_000015.8:g.76681304G= NCBI36
NG_016143.1:g.24389C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326828.6:c.735C= MANE Select ENSP00000315602.5:p.Thr245=
ENST00000326828.5:c.735C= ENSP00000315602.5:p.Thr245=
ENST00000348639.7:c.735C= ENSP00000267951.4:p.Thr245=
ENST00000558903.1:n.442C=
ENST00000559658.5:c.735C= ENSP00000452896.1:p.Thr245=
NM_000743.4:c.735C= NP_000734.2:p.Thr245=
NM_001166694.1:c.735C= NP_001160166.1:p.Thr245=
NR_046313.1:n.1236C=
XM_006720382.1:c.534C= XP_006720445.1:p.Thr178=
XM_011521173.1:c.654C= XP_011519475.1:p.Thr218=
XM_006720382.3:c.534C= XP_006720445.1:p.Thr178=
NM_000743.5:c.735C= MANE Select NP_000734.2:p.Thr245=
NM_001166694.2:c.735C= NP_001160166.1:p.Thr245=
NR_046313.2:n.937C=