Canonical Allele Identifier: CA397802047

Gene: CHRNB1

Linked Data

• MyVariant Identifiers: chr17:g.7359115T>A (hg19) ; chr17:g.7455796T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7455796T>A , CM000679.2:g.7455796T>A	GRCh38
NC_000017.10:g.7359115T>A , CM000679.1:g.7359115T>A	GRCh37
NC_000017.9:g.7299839T>A	NCBI36
NG_008026.1:g.15710T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000306071.7:c.1220T>A MANE Select	ENSP00000304290.2:p.Phe407Tyr
ENST00000306071.6:c.1220T>A	ENSP00000304290.2:p.Phe407Tyr
ENST00000536404.6:c.1004T>A	ENSP00000439209.2:p.Phe335Tyr
ENST00000570557.5:c.883T>A
ENST00000575379.1:c.-173T>A	ENSP00000461751.1:n.-173T>A
ENST00000576360.1:c.857T>A	ENSP00000459092.1:p.Phe286Tyr
NM_000747.2:c.1220T>A	NP_000738.2:p.Phe407Tyr
NM_000747.3:c.1220T>A MANE Select	NP_000738.2:p.Phe407Tyr