Canonical Allele Identifier: CA2189590447
Gene: CHRNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78601999A= , CM000677.2:g.78601999A= GRCh38
NC_000015.9:g.78894341A= , CM000677.1:g.78894341A= GRCh37
NC_000015.8:g.76681396A= NCBI36
NG_016143.1:g.24297T=

Transcript Alleles

HGVS Amino-acid change
ENST00000326828.6:c.643T= MANE Select ENSP00000315602.5:p.Tyr215=
ENST00000326828.5:c.643T= ENSP00000315602.5:p.Tyr215=
ENST00000348639.7:c.643T= ENSP00000267951.4:p.Tyr215=
ENST00000558903.1:n.350T=
ENST00000559658.5:c.643T= ENSP00000452896.1:p.Tyr215=
NM_000743.4:c.643T= NP_000734.2:p.Tyr215=
NM_001166694.1:c.643T= NP_001160166.1:p.Tyr215=
NR_046313.1:n.1144T=
XM_006720382.1:c.442T= XP_006720445.1:p.Tyr148=
XM_011521173.1:c.562T= XP_011519475.1:p.Tyr188=
XM_006720382.3:c.442T= XP_006720445.1:p.Tyr148=
NM_000743.5:c.643T= MANE Select NP_000734.2:p.Tyr215=
NM_001166694.2:c.643T= NP_001160166.1:p.Tyr215=
NR_046313.2:n.845T=