Canonical Allele Identifier: CA393584435
Gene: CHRNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78601706C>G , CM000677.2:g.78601706C>G GRCh38
NC_000015.9:g.78894048C>G , CM000677.1:g.78894048C>G GRCh37
NC_000015.8:g.76681103C>G NCBI36
NG_016143.1:g.24590G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000326828.6:c.936G>C MANE Select ENSP00000315602.5:p.Met312Ile
ENST00000326828.5:c.936G>C ENSP00000315602.5:p.Met312Ile
ENST00000348639.7:c.936G>C ENSP00000267951.4:p.Met312Ile
ENST00000559658.5:c.936G>C ENSP00000452896.1:p.Met312Ile
NM_000743.4:c.936G>C NP_000734.2:p.Met312Ile
NM_001166694.1:c.936G>C NP_001160166.1:p.Met312Ile
NR_046313.1:n.1437G>C
XM_006720382.1:c.735G>C XP_006720445.1:p.Met245Ile
XM_011521173.1:c.855G>C XP_011519475.1:p.Met285Ile
XM_006720382.3:c.735G>C XP_006720445.1:p.Met245Ile
NM_000743.5:c.936G>C MANE Select NP_000734.2:p.Met312Ile
NM_001166694.2:c.936G>C NP_001160166.1:p.Met312Ile
NR_046313.2:n.1138G>C