Canonical Allele Identifier: CA2189589902

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601805G= , CM000677.2:g.78601805G=	GRCh38
NC_000015.9:g.78894147G= , CM000677.1:g.78894147G=	GRCh37
NC_000015.8:g.76681202G=	NCBI36
NG_016143.1:g.24491C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.837C= MANE Select	ENSP00000315602.5:p.Val279=
ENST00000326828.5:c.837C=	ENSP00000315602.5:p.Val279=
ENST00000348639.7:c.837C=	ENSP00000267951.4:p.Val279=
ENST00000558903.1:n.544C=
ENST00000559658.5:c.837C=	ENSP00000452896.1:p.Val279=
NM_000743.4:c.837C=	NP_000734.2:p.Val279=
NM_001166694.1:c.837C=	NP_001160166.1:p.Val279=
NR_046313.1:n.1338C=
XM_006720382.1:c.636C=	XP_006720445.1:p.Val212=
XM_011521173.1:c.756C=	XP_011519475.1:p.Val252=
XM_006720382.3:c.636C=	XP_006720445.1:p.Val212=
NM_000743.5:c.837C= MANE Select	NP_000734.2:p.Val279=
NM_001166694.2:c.837C=	NP_001160166.1:p.Val279=
NR_046313.2:n.1039C=