Canonical Allele Identifier: CA397798860

Gene: CHRNB1

Linked Data

• dbSNP Id: rs2150842456
• MyVariant Identifiers: chr17:g.7357819A>T (hg19) ; chr17:g.7454500A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7454500A>T , CM000679.2:g.7454500A>T	GRCh38
NC_000017.10:g.7357819A>T , CM000679.1:g.7357819A>T	GRCh37
NC_000017.9:g.7298543A>T	NCBI36
NG_008026.1:g.14414A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.1024A>T MANE Select	ENSP00000304290.2:p.Met342Leu
ENST00000306071.6:c.1024A>T	ENSP00000304290.2:p.Met342Leu
ENST00000536404.6:c.808A>T	ENSP00000439209.2:p.Met270Leu
ENST00000570557.5:c.687A>T
ENST00000573209.1:n.1968A>T
ENST00000576360.1:c.661A>T	ENSP00000459092.1:p.Met221Leu
NM_000747.2:c.1024A>T	NP_000738.2:p.Met342Leu
NM_000747.3:c.1024A>T MANE Select	NP_000738.2:p.Met342Leu