Canonical Allele Identifier: CA273900199

Gene: CHRNA3

Linked Data

• dbSNP Id: rs199832016
• gnomAD v4: 15-78595892-A-C
• MyVariant Identifiers: chr15:g.78888234A>C (hg19) ; chr15:g.78595892A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595892A>C , CM000677.2:g.78595892A>C	GRCh38
NC_000015.9:g.78888234A>C , CM000677.1:g.78888234A>C	GRCh37
NC_000015.8:g.76675289A>C	NCBI36
NG_016143.1:g.30404T>G
NG_023328.1:g.35373A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.*712T>G MANE Select	ENSP00000315602.5:n.*712T>G
ENST00000326828.5:c.*712T>G	ENSP00000315602.5:n.*712T>G
ENST00000348639.7:c.1390-2701T>G	ENSP00000267951.4:n.1390-2701T>G
ENST00000559002.5:n.193+648T>G
ENST00000559658.5:c.*64+648T>G	ENSP00000452896.1:n.*64+648T>G
NM_000743.4:c.*712T>G	NP_000734.2:n.*712T>G
NM_001166694.1:c.1390-2701T>G	NP_001160166.1:n.1390-2701T>G
NR_046313.1:n.2083+648T>G
XM_006720382.1:c.*712T>G	XP_006720445.1:n.*712T>G
XM_011521173.1:c.*712T>G	XP_011519475.1:n.*712T>G
XM_006720382.3:c.*712T>G	XP_006720445.1:n.*712T>G
NM_000743.5:c.*712T>G MANE Select	NP_000734.2:n.*712T>G
NM_001166694.2:c.1390-2701T>G	NP_001160166.1:n.1390-2701T>G
NR_046313.2:n.1784+648T>G