Canonical Allele Identifier: CA2629789145

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78617141-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78617141A>C , CM000677.2:g.78617141A>C	GRCh38
NC_000015.9:g.78909483A>C , CM000677.1:g.78909483A>C	GRCh37
NC_000015.8:g.76696538A>C	NCBI36
NG_016143.1:g.9155T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.268-8T>G MANE Select	ENSP00000315602.5:n.268-8T>G
ENST00000326828.5:c.268-8T>G	ENSP00000315602.5:n.268-8T>G
ENST00000348639.7:c.268-8T>G	ENSP00000267951.4:n.268-8T>G
ENST00000559658.5:c.268-8T>G	ENSP00000452896.1:n.268-8T>G
NM_000743.4:c.268-8T>G	NP_000734.2:n.268-8T>G
NM_001166694.1:c.268-8T>G	NP_001160166.1:n.268-8T>G
NR_046313.1:n.769-8T>G
XM_006720382.1:c.67-8T>G	XP_006720445.1:n.67-8T>G
XM_011521173.1:c.187-8T>G	XP_011519475.1:n.187-8T>G
XM_006720382.3:c.67-8T>G	XP_006720445.1:n.67-8T>G
NM_000743.5:c.268-8T>G MANE Select	NP_000734.2:n.268-8T>G
NM_001166694.2:c.268-8T>G	NP_001160166.1:n.268-8T>G
NR_046313.2:n.470-8T>G