Canonical Allele Identifier: CA2189590183
Gene: CHRNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78601922C= , CM000677.2:g.78601922C= GRCh38
NC_000015.9:g.78894264C= , CM000677.1:g.78894264C= GRCh37
NC_000015.8:g.76681319C= NCBI36
NG_016143.1:g.24374G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326828.6:c.720G= MANE Select ENSP00000315602.5:p.Leu240=
ENST00000326828.5:c.720G= ENSP00000315602.5:p.Leu240=
ENST00000348639.7:c.720G= ENSP00000267951.4:p.Leu240=
ENST00000558903.1:n.427G=
ENST00000559658.5:c.720G= ENSP00000452896.1:p.Leu240=
NM_000743.4:c.720G= NP_000734.2:p.Leu240=
NM_001166694.1:c.720G= NP_001160166.1:p.Leu240=
NR_046313.1:n.1221G=
XM_006720382.1:c.519G= XP_006720445.1:p.Leu173=
XM_011521173.1:c.639G= XP_011519475.1:p.Leu213=
XM_006720382.3:c.519G= XP_006720445.1:p.Leu173=
NM_000743.5:c.720G= MANE Select NP_000734.2:p.Leu240=
NM_001166694.2:c.720G= NP_001160166.1:p.Leu240=
NR_046313.2:n.922G=