Canonical Allele Identifier: CA497744608

Gene: CHRNB1

Linked Data

• dbSNP Id: rs1371639390
• MyVariant Identifiers: chr17:g.7357662G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7454343G>T , CM000679.2:g.7454343G>T	GRCh38
NC_000017.10:g.7357662G>T , CM000679.1:g.7357662G>T	GRCh37
NC_000017.9:g.7298386G>T	NCBI36
NG_008026.1:g.14257G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.867G>T MANE Select	ENSP00000304290.2:p.Val289=
ENST00000306071.6:c.867G>T	ENSP00000304290.2:p.Val289=
ENST00000536404.6:c.651G>T	ENSP00000439209.2:p.Val217=
ENST00000570557.5:c.530G>T
ENST00000573209.1:n.1811G>T
ENST00000576360.1:c.605-101G>T	ENSP00000459092.1:n.605-101G>T
NM_000747.2:c.867G>T	NP_000738.2:p.Val289=
NM_000747.3:c.867G>T MANE Select	NP_000738.2:p.Val289=