Canonical Allele Identifier: CA2189603521

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78618852A= , CM000677.2:g.78618852A=	GRCh38
NC_000015.9:g.78911194A= , CM000677.1:g.78911194A=	GRCh37
NC_000015.8:g.76698249A=	NCBI36
NG_016143.1:g.7444T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.146T= MANE Select	ENSP00000315602.5:p.Ile49=
ENST00000326828.5:c.146T=	ENSP00000315602.5:p.Ile49=
ENST00000348639.7:c.146T=	ENSP00000267951.4:p.Ile49=
ENST00000559080.1:c.-56T=	ENSP00000453993.1:n.-56T=
ENST00000559658.5:c.146T=	ENSP00000452896.1:p.Ile49=
ENST00000559941.1:n.589T=
ENST00000561128.1:n.141T=
NM_000743.4:c.146T=	NP_000734.2:p.Ile49=
NM_001166694.1:c.146T=	NP_001160166.1:p.Ile49=
NR_046313.1:n.647T=
XM_006720382.1:c.-56T=	XP_006720445.1:n.-56T=
XM_011521173.1:c.65T=	XP_011519475.1:p.Ile22=
XM_006720382.3:c.-56T=	XP_006720445.1:n.-56T=
NM_000743.5:c.146T= MANE Select	NP_000734.2:p.Ile49=
NM_001166694.2:c.146T=	NP_001160166.1:p.Ile49=
NR_046313.2:n.348T=