Canonical Allele Identifier: CA2189603520

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78618847G= , CM000677.2:g.78618847G=	GRCh38
NC_000015.9:g.78911189G= , CM000677.1:g.78911189G=	GRCh37
NC_000015.8:g.76698244G=	NCBI36
NG_016143.1:g.7449C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.151C= MANE Select	ENSP00000315602.5:p.Arg51=
ENST00000326828.5:c.151C=	ENSP00000315602.5:p.Arg51=
ENST00000348639.7:c.151C=	ENSP00000267951.4:p.Arg51=
ENST00000559080.1:c.-51C=	ENSP00000453993.1:n.-51C=
ENST00000559658.5:c.151C=	ENSP00000452896.1:p.Arg51=
ENST00000561128.1:n.146C=
NM_000743.4:c.151C=	NP_000734.2:p.Arg51=
NM_001166694.1:c.151C=	NP_001160166.1:p.Arg51=
NR_046313.1:n.652C=
XM_006720382.1:c.-51C=	XP_006720445.1:n.-51C=
XM_011521173.1:c.70C=	XP_011519475.1:p.Arg24=
XM_006720382.3:c.-51C=	XP_006720445.1:n.-51C=
NM_000743.5:c.151C= MANE Select	NP_000734.2:p.Arg51=
NM_001166694.2:c.151C=	NP_001160166.1:p.Arg51=
NR_046313.2:n.353C=