Canonical Allele Identifier: CA497745007
Gene: CHRNB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7359200G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7455881G>A , CM000679.2:g.7455881G>A GRCh38
NC_000017.10:g.7359200G>A , CM000679.1:g.7359200G>A GRCh37
NC_000017.9:g.7299924G>A NCBI36
NG_008026.1:g.15795G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000306071.7:c.1305G>A MANE Select ENSP00000304290.2:p.Glu435=
ENST00000306071.6:c.1305G>A ENSP00000304290.2:p.Glu435=
ENST00000536404.6:c.1089G>A ENSP00000439209.2:p.Glu363=
ENST00000575379.1:c.-88G>A ENSP00000461751.1:n.-88G>A
ENST00000576360.1:c.942G>A ENSP00000459092.1:p.Glu314=
NM_000747.2:c.1305G>A NP_000738.2:p.Glu435=
NM_000747.3:c.1305G>A MANE Select NP_000738.2:p.Glu435=
Search 100 bp 5'
Search 100 bp 3'