Canonical Allele Identifier: CA2189585464
Gene: CHRNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78599226C= , CM000677.2:g.78599226C= GRCh38
NC_000015.9:g.78891568C= , CM000677.1:g.78891568C= GRCh37
NC_000015.8:g.76678623C= NCBI36
NG_016143.1:g.27070G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326828.6:c.1389+2027G= MANE Select ENSP00000315602.5:n.1389+2027G=
ENST00000326828.5:c.1389+2027G= ENSP00000315602.5:n.1389+2027G=
ENST00000348639.7:c.1389+2027G= ENSP00000267951.4:n.1389+2027G=
ENST00000559658.5:c.1389+2027G= ENSP00000452896.1:n.1389+2027G=
NM_000743.4:c.1389+2027G= NP_000734.2:n.1389+2027G=
NM_001166694.1:c.1389+2027G= NP_001160166.1:n.1389+2027G=
NR_046313.1:n.1890+2027G=
XM_006720382.1:c.1188+2027G= XP_006720445.1:n.1188+2027G=
XM_011521173.1:c.1308+2027G= XP_011519475.1:n.1308+2027G=
XM_006720382.3:c.1188+2027G= XP_006720445.1:n.1188+2027G=
NM_000743.5:c.1389+2027G= MANE Select NP_000734.2:n.1389+2027G=
NM_001166694.2:c.1389+2027G= NP_001160166.1:n.1389+2027G=
NR_046313.2:n.1591+2027G=