Canonical Allele Identifier: CA2629793195
Gene: CHRNA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78595885A>T , CM000677.2:g.78595885A>T GRCh38
NC_000015.9:g.78888227A>T , CM000677.1:g.78888227A>T GRCh37
NC_000015.8:g.76675282A>T NCBI36
NG_016143.1:g.30411T>A
NG_023328.1:g.35366A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000326828.6:c.*719T>A MANE Select ENSP00000315602.5:n.*719T>A
ENST00000326828.5:c.*719T>A ENSP00000315602.5:n.*719T>A
ENST00000348639.7:c.1390-2694T>A ENSP00000267951.4:n.1390-2694T>A
ENST00000559002.5:n.193+655T>A
ENST00000559658.5:c.*64+655T>A ENSP00000452896.1:n.*64+655T>A
NM_000743.4:c.*719T>A NP_000734.2:n.*719T>A
NM_001166694.1:c.1390-2694T>A NP_001160166.1:n.1390-2694T>A
NR_046313.1:n.2083+655T>A
XM_006720382.1:c.*719T>A XP_006720445.1:n.*719T>A
XM_011521173.1:c.*719T>A XP_011519475.1:n.*719T>A
XM_006720382.3:c.*719T>A XP_006720445.1:n.*719T>A
NM_000743.5:c.*719T>A MANE Select NP_000734.2:n.*719T>A
NM_001166694.2:c.1390-2694T>A NP_001160166.1:n.1390-2694T>A
NR_046313.2:n.1784+655T>A