Canonical Allele Identifier: CA2189591393

Gene: CHRNA3

Linked Data

• dbSNP Id: rs2053221069

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602454_78602457del , CM000677.2:g.78602454_78602457del	GRCh38
NC_000015.9:g.78894796_78894799del , CM000677.1:g.78894796_78894799del	GRCh37
NC_000015.8:g.76681851_76681854del	NCBI36
NG_016143.1:g.23844_23847del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.378-188_378-185del MANE Select	ENSP00000315602.5:n.378-188_378-185del
ENST00000326828.5:c.378-188_378-185del	ENSP00000315602.5:n.378-188_378-185del
ENST00000348639.7:c.378-188_378-185del	ENSP00000267951.4:n.378-188_378-185del
ENST00000558903.1:n.85-188_85-185del
ENST00000559658.5:c.378-188_378-185del	ENSP00000452896.1:n.378-188_378-185del
NM_000743.4:c.378-188_378-185del	NP_000734.2:n.378-188_378-185del
NM_001166694.1:c.378-188_378-185del	NP_001160166.1:n.378-188_378-185del
NR_046313.1:n.879-188_879-185del
XM_006720382.1:c.177-188_177-185del	XP_006720445.1:n.177-188_177-185del
XM_011521173.1:c.297-188_297-185del	XP_011519475.1:n.297-188_297-185del
XM_006720382.3:c.177-188_177-185del	XP_006720445.1:n.177-188_177-185del
NM_000743.5:c.378-188_378-185del MANE Select	NP_000734.2:n.378-188_378-185del
NM_001166694.2:c.378-188_378-185del	NP_001160166.1:n.378-188_378-185del
NR_046313.2:n.580-188_580-185del