Canonical Allele Identifier: CA497744728
Gene: CHRNB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7357836T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454517T>A , CM000679.2:g.7454517T>A GRCh38
NC_000017.10:g.7357836T>A , CM000679.1:g.7357836T>A GRCh37
NC_000017.9:g.7298560T>A NCBI36
NG_008026.1:g.14431T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1041T>A MANE Select ENSP00000304290.2:p.Arg347=
ENST00000306071.6:c.1041T>A ENSP00000304290.2:p.Arg347=
ENST00000536404.6:c.825T>A ENSP00000439209.2:p.Arg275=
ENST00000570557.5:c.704T>A
ENST00000573209.1:n.1985T>A
ENST00000576360.1:c.678T>A ENSP00000459092.1:p.Arg226=
NM_000747.2:c.1041T>A NP_000738.2:p.Arg347=
NM_000747.3:c.1041T>A MANE Select NP_000738.2:p.Arg347=