Canonical Allele Identifier: CA397800843
Gene: CHRNB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7358683C>A (hg19) chr17:g.7455364C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7455364C>A , CM000679.2:g.7455364C>A GRCh38
NC_000017.10:g.7358683C>A , CM000679.1:g.7358683C>A GRCh37
NC_000017.9:g.7299407C>A NCBI36
NG_008026.1:g.15278C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1125C>A MANE Select ENSP00000304290.2:p.His375Gln
ENST00000306071.6:c.1125C>A ENSP00000304290.2:p.His375Gln
ENST00000536404.6:c.909C>A ENSP00000439209.2:p.His303Gln
ENST00000570557.5:c.788C>A
ENST00000573209.1:n.2069C>A
ENST00000576360.1:c.762C>A ENSP00000459092.1:p.His254Gln
NM_000747.2:c.1125C>A NP_000738.2:p.His375Gln
NM_000747.3:c.1125C>A MANE Select NP_000738.2:p.His375Gln
Search 100 bp 5'
Search 100 bp 3'