Canonical Allele Identifier: CA2245821878

Gene: CHRNB1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7454448C= , CM000679.2:g.7454448C=	GRCh38
NC_000017.10:g.7357767C= , CM000679.1:g.7357767C=	GRCh37
NC_000017.9:g.7298491C=	NCBI36
NG_008026.1:g.14362C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.972C= MANE Select	ENSP00000304290.2:p.Ile324=
ENST00000306071.6:c.972C=	ENSP00000304290.2:p.Ile324=
ENST00000536404.6:c.756C=	ENSP00000439209.2:p.Ile252=
ENST00000570557.5:c.635C=
ENST00000573209.1:n.1916C=
ENST00000576360.1:c.609C=	ENSP00000459092.1:p.Ile203=
NM_000747.2:c.972C=	NP_000738.2:p.Ile324=
NM_000747.3:c.972C= MANE Select	NP_000738.2:p.Ile324=