Canonical Allele Identifier: CA393585104

Gene: CHRNA3

Linked Data

• dbSNP Id: rs2053208892
• gnomAD v3: 15-78601935-T-C
• gnomAD v4: 15-78601935-T-C
• MyVariant Identifiers: chr15:g.78894277T>C (hg19) ; chr15:g.78601935T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601935T>C , CM000677.2:g.78601935T>C	GRCh38
NC_000015.9:g.78894277T>C , CM000677.1:g.78894277T>C	GRCh37
NC_000015.8:g.76681332T>C	NCBI36
NG_016143.1:g.24361A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.707A>G MANE Select	ENSP00000315602.5:p.Tyr236Cys
ENST00000326828.5:c.707A>G	ENSP00000315602.5:p.Tyr236Cys
ENST00000348639.7:c.707A>G	ENSP00000267951.4:p.Tyr236Cys
ENST00000558903.1:n.414A>G
ENST00000559658.5:c.707A>G	ENSP00000452896.1:p.Tyr236Cys
NM_000743.4:c.707A>G	NP_000734.2:p.Tyr236Cys
NM_001166694.1:c.707A>G	NP_001160166.1:p.Tyr236Cys
NR_046313.1:n.1208A>G
XM_006720382.1:c.506A>G	XP_006720445.1:p.Tyr169Cys
XM_011521173.1:c.626A>G	XP_011519475.1:p.Tyr209Cys
XM_006720382.3:c.506A>G	XP_006720445.1:p.Tyr169Cys
NM_000743.5:c.707A>G MANE Select	NP_000734.2:p.Tyr236Cys
NM_001166694.2:c.707A>G	NP_001160166.1:p.Tyr236Cys
NR_046313.2:n.909A>G