Canonical Allele Identifier: CA2189601828
Gene: CHRNA3 HGNC NCBI

Linked Data

dbSNP Id: rs961115712

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78615600C>G , CM000677.2:g.78615600C>G GRCh38
NC_000015.9:g.78907942C>G , CM000677.1:g.78907942C>G GRCh37
NC_000015.8:g.76694997C>G NCBI36
NG_016143.1:g.10696G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000326828.6:c.377+1424G>C MANE Select ENSP00000315602.5:n.377+1424G>C
ENST00000326828.5:c.377+1424G>C ENSP00000315602.5:n.377+1424G>C
ENST00000348639.7:c.377+1424G>C ENSP00000267951.4:n.377+1424G>C
ENST00000559658.5:c.377+1424G>C ENSP00000452896.1:n.377+1424G>C
NM_000743.4:c.377+1424G>C NP_000734.2:n.377+1424G>C
NM_001166694.1:c.377+1424G>C NP_001160166.1:n.377+1424G>C
NR_046313.1:n.878+1424G>C
XM_006720382.1:c.176+1424G>C XP_006720445.1:n.176+1424G>C
XM_011521173.1:c.296+1424G>C XP_011519475.1:n.296+1424G>C
XM_006720382.3:c.176+1424G>C XP_006720445.1:n.176+1424G>C
NM_000743.5:c.377+1424G>C MANE Select NP_000734.2:n.377+1424G>C
NM_001166694.2:c.377+1424G>C NP_001160166.1:n.377+1424G>C
NR_046313.2:n.579+1424G>C