Canonical Allele Identifier: CA7684467
Gene: CHRNA3 HGNC NCBI

Linked Data

dbSNP Id: rs762582486

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78602158C>T , CM000677.2:g.78602158C>T GRCh38
NC_000015.9:g.78894500C>T , CM000677.1:g.78894500C>T GRCh37
NC_000015.8:g.76681555C>T NCBI36
NG_016143.1:g.24138G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326828.6:c.484G>A MANE Select ENSP00000315602.5:p.Asp162Asn
ENST00000326828.5:c.484G>A ENSP00000315602.5:p.Asp162Asn
ENST00000348639.7:c.484G>A ENSP00000267951.4:p.Asp162Asn
ENST00000558903.1:n.191G>A
ENST00000559658.5:c.484G>A ENSP00000452896.1:p.Asp162Asn
NM_000743.4:c.484G>A NP_000734.2:p.Asp162Asn
NM_001166694.1:c.484G>A NP_001160166.1:p.Asp162Asn
NR_046313.1:n.985G>A
XM_006720382.1:c.283G>A XP_006720445.1:p.Asp95Asn
XM_011521173.1:c.403G>A XP_011519475.1:p.Asp135Asn
XM_006720382.3:c.283G>A XP_006720445.1:p.Asp95Asn
NM_000743.5:c.484G>A MANE Select NP_000734.2:p.Asp162Asn
NM_001166694.2:c.484G>A NP_001160166.1:p.Asp162Asn
NR_046313.2:n.686G>A