Canonical Allele Identifier: CA2189590300

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601949G= , CM000677.2:g.78601949G=	GRCh38
NC_000015.9:g.78894291G= , CM000677.1:g.78894291G=	GRCh37
NC_000015.8:g.76681346G=	NCBI36
NG_016143.1:g.24347C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.693C= MANE Select	ENSP00000315602.5:p.Ile231=
ENST00000326828.5:c.693C=	ENSP00000315602.5:p.Ile231=
ENST00000348639.7:c.693C=	ENSP00000267951.4:p.Ile231=
ENST00000558903.1:n.400C=
ENST00000559658.5:c.693C=	ENSP00000452896.1:p.Ile231=
NM_000743.4:c.693C=	NP_000734.2:p.Ile231=
NM_001166694.1:c.693C=	NP_001160166.1:p.Ile231=
NR_046313.1:n.1194C=
XM_006720382.1:c.492C=	XP_006720445.1:p.Ile164=
XM_011521173.1:c.612C=	XP_011519475.1:p.Ile204=
XM_006720382.3:c.492C=	XP_006720445.1:p.Ile164=
NM_000743.5:c.693C= MANE Select	NP_000734.2:p.Ile231=
NM_001166694.2:c.693C=	NP_001160166.1:p.Ile231=
NR_046313.2:n.895C=