Canonical Allele Identifier: CA2189591471

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602535T= , CM000677.2:g.78602535T=	GRCh38
NC_000015.9:g.78894877T= , CM000677.1:g.78894877T=	GRCh37
NC_000015.8:g.76681932T=	NCBI36
NG_016143.1:g.23761A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.378-271A= MANE Select	ENSP00000315602.5:n.378-271A=
ENST00000326828.5:c.378-271A=	ENSP00000315602.5:n.378-271A=
ENST00000348639.7:c.378-271A=	ENSP00000267951.4:n.378-271A=
ENST00000558903.1:n.85-271A=
ENST00000559658.5:c.378-271A=	ENSP00000452896.1:n.378-271A=
NM_000743.4:c.378-271A=	NP_000734.2:n.378-271A=
NM_001166694.1:c.378-271A=	NP_001160166.1:n.378-271A=
NR_046313.1:n.879-271A=
XM_006720382.1:c.177-271A=	XP_006720445.1:n.177-271A=
XM_011521173.1:c.297-271A=	XP_011519475.1:n.297-271A=
XM_006720382.3:c.177-271A=	XP_006720445.1:n.177-271A=
NM_000743.5:c.378-271A= MANE Select	NP_000734.2:n.378-271A=
NM_001166694.2:c.378-271A=	NP_001160166.1:n.378-271A=
NR_046313.2:n.580-271A=