Canonical Allele Identifier: CA7684430
Gene: CHRNA3 HGNC NCBI

Linked Data

dbSNP Id: rs759093187

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78602009T>A , CM000677.2:g.78602009T>A GRCh38
NC_000015.9:g.78894351T>A , CM000677.1:g.78894351T>A GRCh37
NC_000015.8:g.76681406T>A NCBI36
NG_016143.1:g.24287A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000326828.6:c.633A>T MANE Select ENSP00000315602.5:p.Lys211Asn
ENST00000326828.5:c.633A>T ENSP00000315602.5:p.Lys211Asn
ENST00000348639.7:c.633A>T ENSP00000267951.4:p.Lys211Asn
ENST00000558903.1:n.340A>T
ENST00000559658.5:c.633A>T ENSP00000452896.1:p.Lys211Asn
NM_000743.4:c.633A>T NP_000734.2:p.Lys211Asn
NM_001166694.1:c.633A>T NP_001160166.1:p.Lys211Asn
NR_046313.1:n.1134A>T
XM_006720382.1:c.432A>T XP_006720445.1:p.Lys144Asn
XM_011521173.1:c.552A>T XP_011519475.1:p.Lys184Asn
XM_006720382.3:c.432A>T XP_006720445.1:p.Lys144Asn
NM_000743.5:c.633A>T MANE Select NP_000734.2:p.Lys211Asn
NM_001166694.2:c.633A>T NP_001160166.1:p.Lys211Asn
NR_046313.2:n.835A>T