Canonical Allele Identifier: CA1779564251

Gene: CHRNB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42732528G= , CM000670.2:g.42732528G=	GRCh38
NC_000008.10:g.42587671G= , CM000670.1:g.42587671G=	GRCh37
NC_000008.9:g.42706828G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289957.3:c.1221G= MANE Select	ENSP00000289957.2:p.Lys407=
ENST00000289957.2:c.1221G=	ENSP00000289957.2:p.Lys407=
NM_000749.3:c.1221G=	NP_000740.1:p.Lys407=
XM_011544390.1:c.834G=	XP_011542692.1:p.Lys278=
NM_000749.4:c.1221G=	NP_000740.1:p.Lys407=
NM_001347717.1:c.999G=	NP_001334646.1:p.Lys333=
XM_011544390.2:c.834G=	XP_011542692.1:p.Lys278=
NM_000749.5:c.1221G= MANE Select	NP_000740.1:p.Lys407=
NM_001347717.2:c.999G=	NP_001334646.1:p.Lys333=