Canonical Allele Identifier: CA273905248
Gene: CHRNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78601585C>T , CM000677.2:g.78601585C>T GRCh38
NC_000015.9:g.78893927C>T , CM000677.1:g.78893927C>T GRCh37
NC_000015.8:g.76680982C>T NCBI36
NG_016143.1:g.24711G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326828.6:c.1057G>A MANE Select ENSP00000315602.5:p.Val353Ile
ENST00000326828.5:c.1057G>A ENSP00000315602.5:p.Val353Ile
ENST00000348639.7:c.1057G>A ENSP00000267951.4:p.Val353Ile
ENST00000559658.5:c.1057G>A ENSP00000452896.1:p.Val353Ile
NM_000743.4:c.1057G>A NP_000734.2:p.Val353Ile
NM_001166694.1:c.1057G>A NP_001160166.1:p.Val353Ile
NR_046313.1:n.1558G>A
XM_006720382.1:c.856G>A XP_006720445.1:p.Val286Ile
XM_011521173.1:c.976G>A XP_011519475.1:p.Val326Ile
XM_006720382.3:c.856G>A XP_006720445.1:p.Val286Ile
NM_000743.5:c.1057G>A MANE Select NP_000734.2:p.Val353Ile
NM_001166694.2:c.1057G>A NP_001160166.1:p.Val353Ile
NR_046313.2:n.1259G>A