Canonical Allele Identifier: CA393586004
Gene: CHRNA3 HGNC NCBI

Linked Data

dbSNP Id: rs2053214068
COSMIC: COSM965402

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78602139A>G , CM000677.2:g.78602139A>G GRCh38
NC_000015.9:g.78894481A>G , CM000677.1:g.78894481A>G GRCh37
NC_000015.8:g.76681536A>G NCBI36
NG_016143.1:g.24157T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000326828.6:c.503T>C MANE Select ENSP00000315602.5:p.Phe168Ser
ENST00000326828.5:c.503T>C ENSP00000315602.5:p.Phe168Ser
ENST00000348639.7:c.503T>C ENSP00000267951.4:p.Phe168Ser
ENST00000558903.1:n.210T>C
ENST00000559658.5:c.503T>C ENSP00000452896.1:p.Phe168Ser
NM_000743.4:c.503T>C NP_000734.2:p.Phe168Ser
NM_001166694.1:c.503T>C NP_001160166.1:p.Phe168Ser
NR_046313.1:n.1004T>C
XM_006720382.1:c.302T>C XP_006720445.1:p.Phe101Ser
XM_011521173.1:c.422T>C XP_011519475.1:p.Phe141Ser
XM_006720382.3:c.302T>C XP_006720445.1:p.Phe101Ser
NM_000743.5:c.503T>C MANE Select NP_000734.2:p.Phe168Ser
NM_001166694.2:c.503T>C NP_001160166.1:p.Phe168Ser
NR_046313.2:n.705T>C