Canonical Allele Identifier: CA397802622
Gene: CHRNB1 HGNC NCBI

Linked Data

COSMIC: COSM4413002
MyVariant Identifiers: chr17:g.7359200G>C (hg19) chr17:g.7455881G>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000306071.7:c.1305G>C MANE Select ENSP00000304290.2:p.Glu435Asp
ENST00000306071.6:c.1305G>C ENSP00000304290.2:p.Glu435Asp
ENST00000536404.6:c.1089G>C ENSP00000439209.2:p.Glu363Asp
ENST00000575379.1:c.-88G>C ENSP00000461751.1:n.-88G>C
ENST00000576360.1:c.942G>C ENSP00000459092.1:p.Glu314Asp
NM_000747.2:c.1305G>C NP_000738.2:p.Glu435Asp
NM_000747.3:c.1305G>C MANE Select NP_000738.2:p.Glu435Asp
Search 100 bp 5'
Search 100 bp 3'