Canonical Allele Identifier: CA2245821897

Gene: CHRNB1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7454489A= , CM000679.2:g.7454489A=	GRCh38
NC_000017.10:g.7357808A= , CM000679.1:g.7357808A=	GRCh37
NC_000017.9:g.7298532A=	NCBI36
NG_008026.1:g.14403A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.1013A= MANE Select	ENSP00000304290.2:p.His338=
ENST00000306071.6:c.1013A=	ENSP00000304290.2:p.His338=
ENST00000536404.6:c.797A=	ENSP00000439209.2:p.His266=
ENST00000570557.5:c.676A=
ENST00000573209.1:n.1957A=
ENST00000576360.1:c.650A=	ENSP00000459092.1:p.His217=
NM_000747.2:c.1013A=	NP_000738.2:p.His338=
NM_000747.3:c.1013A= MANE Select	NP_000738.2:p.His338=