Canonical Allele Identifier: CA2629793611

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78596062-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78596062T>C , CM000677.2:g.78596062T>C	GRCh38
NC_000015.9:g.78888404T>C , CM000677.1:g.78888404T>C	GRCh37
NC_000015.8:g.76675459T>C	NCBI36
NG_016143.1:g.30234A>G
NG_023328.1:g.35543T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.*542A>G MANE Select	ENSP00000315602.5:n.*542A>G
ENST00000326828.5:c.*542A>G	ENSP00000315602.5:n.*542A>G
ENST00000348639.7:c.1390-2871A>G	ENSP00000267951.4:n.1390-2871A>G
ENST00000559002.5:n.193+478A>G
ENST00000559658.5:c.*64+478A>G	ENSP00000452896.1:n.*64+478A>G
NM_000743.4:c.*542A>G	NP_000734.2:n.*542A>G
NM_001166694.1:c.1390-2871A>G	NP_001160166.1:n.1390-2871A>G
NR_046313.1:n.2083+478A>G
XM_006720382.1:c.*542A>G	XP_006720445.1:n.*542A>G
XM_011521173.1:c.*542A>G	XP_011519475.1:n.*542A>G
XM_006720382.3:c.*542A>G	XP_006720445.1:n.*542A>G
NM_000743.5:c.*542A>G MANE Select	NP_000734.2:n.*542A>G
NM_001166694.2:c.1390-2871A>G	NP_001160166.1:n.1390-2871A>G
NR_046313.2:n.1784+478A>G