Canonical Allele Identifier: CA2557530801
Gene: CHRNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78615576G>T , CM000677.2:g.78615576G>T GRCh38
NC_000015.9:g.78907918G>T , CM000677.1:g.78907918G>T GRCh37
NC_000015.8:g.76694973G>T NCBI36
NG_016143.1:g.10720C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326828.6:c.377+1448C>A MANE Select ENSP00000315602.5:n.377+1448C>A
ENST00000326828.5:c.377+1448C>A ENSP00000315602.5:n.377+1448C>A
ENST00000348639.7:c.377+1448C>A ENSP00000267951.4:n.377+1448C>A
ENST00000559658.5:c.377+1448C>A ENSP00000452896.1:n.377+1448C>A
NM_000743.4:c.377+1448C>A NP_000734.2:n.377+1448C>A
NM_001166694.1:c.377+1448C>A NP_001160166.1:n.377+1448C>A
NR_046313.1:n.878+1448C>A
XM_006720382.1:c.176+1448C>A XP_006720445.1:n.176+1448C>A
XM_011521173.1:c.296+1448C>A XP_011519475.1:n.296+1448C>A
XM_006720382.3:c.176+1448C>A XP_006720445.1:n.176+1448C>A
NM_000743.5:c.377+1448C>A MANE Select NP_000734.2:n.377+1448C>A
NM_001166694.2:c.377+1448C>A NP_001160166.1:n.377+1448C>A
NR_046313.2:n.579+1448C>A