Canonical Allele Identifier: CA2189602578

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78617054A= , CM000677.2:g.78617054A=	GRCh38
NC_000015.9:g.78909396A= , CM000677.1:g.78909396A=	GRCh37
NC_000015.8:g.76696451A=	NCBI36
NG_016143.1:g.9242T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.347T= MANE Select	ENSP00000315602.5:p.Ile116=
ENST00000326828.5:c.347T=	ENSP00000315602.5:p.Ile116=
ENST00000348639.7:c.347T=	ENSP00000267951.4:p.Ile116=
ENST00000559658.5:c.347T=	ENSP00000452896.1:p.Ile116=
NM_000743.4:c.347T=	NP_000734.2:p.Ile116=
NM_001166694.1:c.347T=	NP_001160166.1:p.Ile116=
NR_046313.1:n.848T=
XM_006720382.1:c.146T=	XP_006720445.1:p.Ile49=
XM_011521173.1:c.266T=	XP_011519475.1:p.Ile89=
XM_006720382.3:c.146T=	XP_006720445.1:p.Ile49=
NM_000743.5:c.347T= MANE Select	NP_000734.2:p.Ile116=
NM_001166694.2:c.347T=	NP_001160166.1:p.Ile116=
NR_046313.2:n.549T=