Canonical Allele Identifier: CA273900179
Gene: CHRNA3 HGNC NCBI

Linked Data

dbSNP Id: rs201569881

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78595874A>C , CM000677.2:g.78595874A>C GRCh38
NC_000015.9:g.78888216A>C , CM000677.1:g.78888216A>C GRCh37
NC_000015.8:g.76675271A>C NCBI36
NG_016143.1:g.30422T>G
NG_023328.1:g.35355A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000326828.6:c.*730T>G MANE Select ENSP00000315602.5:n.*730T>G
ENST00000326828.5:c.*730T>G ENSP00000315602.5:n.*730T>G
ENST00000348639.7:c.1390-2683T>G ENSP00000267951.4:n.1390-2683T>G
ENST00000559002.5:n.193+666T>G
ENST00000559658.5:c.*64+666T>G ENSP00000452896.1:n.*64+666T>G
NM_000743.4:c.*730T>G NP_000734.2:n.*730T>G
NM_001166694.1:c.1390-2683T>G NP_001160166.1:n.1390-2683T>G
NR_046313.1:n.2083+666T>G
XM_006720382.1:c.*730T>G XP_006720445.1:n.*730T>G
XM_011521173.1:c.*730T>G XP_011519475.1:n.*730T>G
XM_006720382.3:c.*730T>G XP_006720445.1:n.*730T>G
NM_000743.5:c.*730T>G MANE Select NP_000734.2:n.*730T>G
NM_001166694.2:c.1390-2683T>G NP_001160166.1:n.1390-2683T>G
NR_046313.2:n.1784+666T>G