Canonical Allele Identifier: CA393585511
Gene: CHRNA3 HGNC NCBI

Linked Data

dbSNP Id: rs200382777

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78601990C>A , CM000677.2:g.78601990C>A GRCh38
NC_000015.9:g.78894332C>A , CM000677.1:g.78894332C>A GRCh37
NC_000015.8:g.76681387C>A NCBI36
NG_016143.1:g.24306G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000326828.6:c.652G>T MANE Select ENSP00000315602.5:p.Asp218Tyr
ENST00000326828.5:c.652G>T ENSP00000315602.5:p.Asp218Tyr
ENST00000348639.7:c.652G>T ENSP00000267951.4:p.Asp218Tyr
ENST00000558903.1:n.359G>T
ENST00000559658.5:c.652G>T ENSP00000452896.1:p.Asp218Tyr
NM_000743.4:c.652G>T NP_000734.2:p.Asp218Tyr
NM_001166694.1:c.652G>T NP_001160166.1:p.Asp218Tyr
NR_046313.1:n.1153G>T
XM_006720382.1:c.451G>T XP_006720445.1:p.Asp151Tyr
XM_011521173.1:c.571G>T XP_011519475.1:p.Asp191Tyr
XM_006720382.3:c.451G>T XP_006720445.1:p.Asp151Tyr
NM_000743.5:c.652G>T MANE Select NP_000734.2:p.Asp218Tyr
NM_001166694.2:c.652G>T NP_001160166.1:p.Asp218Tyr
NR_046313.2:n.854G>T