Canonical Allele Identifier: CA2189602629

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78617157A= , CM000677.2:g.78617157A=	GRCh38
NC_000015.9:g.78909499A= , CM000677.1:g.78909499A=	GRCh37
NC_000015.8:g.76696554A=	NCBI36
NG_016143.1:g.9139T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.268-24T= MANE Select	ENSP00000315602.5:n.268-24T=
ENST00000326828.5:c.268-24T=	ENSP00000315602.5:n.268-24T=
ENST00000348639.7:c.268-24T=	ENSP00000267951.4:n.268-24T=
ENST00000559658.5:c.268-24T=	ENSP00000452896.1:n.268-24T=
NM_000743.4:c.268-24T=	NP_000734.2:n.268-24T=
NM_001166694.1:c.268-24T=	NP_001160166.1:n.268-24T=
NR_046313.1:n.769-24T=
XM_006720382.1:c.67-24T=	XP_006720445.1:n.67-24T=
XM_011521173.1:c.187-24T=	XP_011519475.1:n.187-24T=
XM_006720382.3:c.67-24T=	XP_006720445.1:n.67-24T=
NM_000743.5:c.268-24T= MANE Select	NP_000734.2:n.268-24T=
NM_001166694.2:c.268-24T=	NP_001160166.1:n.268-24T=
NR_046313.2:n.470-24T=