Canonical Allele Identifier: CA2189591412

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602461C= , CM000677.2:g.78602461C=	GRCh38
NC_000015.9:g.78894803C= , CM000677.1:g.78894803C=	GRCh37
NC_000015.8:g.76681858C=	NCBI36
NG_016143.1:g.23835G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.378-197G= MANE Select	ENSP00000315602.5:n.378-197G=
ENST00000326828.5:c.378-197G=	ENSP00000315602.5:n.378-197G=
ENST00000348639.7:c.378-197G=	ENSP00000267951.4:n.378-197G=
ENST00000558903.1:n.85-197G=
ENST00000559658.5:c.378-197G=	ENSP00000452896.1:n.378-197G=
NM_000743.4:c.378-197G=	NP_000734.2:n.378-197G=
NM_001166694.1:c.378-197G=	NP_001160166.1:n.378-197G=
NR_046313.1:n.879-197G=
XM_006720382.1:c.177-197G=	XP_006720445.1:n.177-197G=
XM_011521173.1:c.297-197G=	XP_011519475.1:n.297-197G=
XM_006720382.3:c.177-197G=	XP_006720445.1:n.177-197G=
NM_000743.5:c.378-197G= MANE Select	NP_000734.2:n.378-197G=
NM_001166694.2:c.378-197G=	NP_001160166.1:n.378-197G=
NR_046313.2:n.580-197G=