Canonical Allele Identifier: CA2189585601
Gene: CHRNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78599318C= , CM000677.2:g.78599318C= GRCh38
NC_000015.9:g.78891660C= , CM000677.1:g.78891660C= GRCh37
NC_000015.8:g.76678715C= NCBI36
NG_016143.1:g.26978G=

Transcript Alleles

HGVS Amino-acid change
ENST00000326828.6:c.1389+1935G= MANE Select ENSP00000315602.5:n.1389+1935G=
ENST00000326828.5:c.1389+1935G= ENSP00000315602.5:n.1389+1935G=
ENST00000348639.7:c.1389+1935G= ENSP00000267951.4:n.1389+1935G=
ENST00000559658.5:c.1389+1935G= ENSP00000452896.1:n.1389+1935G=
NM_000743.4:c.1389+1935G= NP_000734.2:n.1389+1935G=
NM_001166694.1:c.1389+1935G= NP_001160166.1:n.1389+1935G=
NR_046313.1:n.1890+1935G=
XM_006720382.1:c.1188+1935G= XP_006720445.1:n.1188+1935G=
XM_011521173.1:c.1308+1935G= XP_011519475.1:n.1308+1935G=
XM_006720382.3:c.1188+1935G= XP_006720445.1:n.1188+1935G=
NM_000743.5:c.1389+1935G= MANE Select NP_000734.2:n.1389+1935G=
NM_001166694.2:c.1389+1935G= NP_001160166.1:n.1389+1935G=
NR_046313.2:n.1591+1935G=