Canonical Allele Identifier: CA497744779
Gene: CHRNB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7358677C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7455358C>A , CM000679.2:g.7455358C>A GRCh38
NC_000017.10:g.7358677C>A , CM000679.1:g.7358677C>A GRCh37
NC_000017.9:g.7299401C>A NCBI36
NG_008026.1:g.15272C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000306071.7:c.1119C>A MANE Select ENSP00000304290.2:p.Pro373=
ENST00000306071.6:c.1119C>A ENSP00000304290.2:p.Pro373=
ENST00000536404.6:c.903C>A ENSP00000439209.2:p.Pro301=
ENST00000570557.5:c.782C>A
ENST00000573209.1:n.2063C>A
ENST00000576360.1:c.756C>A ENSP00000459092.1:p.Pro252=
NM_000747.2:c.1119C>A NP_000738.2:p.Pro373=
NM_000747.3:c.1119C>A MANE Select NP_000738.2:p.Pro373=
Search 100 bp 5'
Search 100 bp 3'