Canonical Allele Identifier: CA2189602615

Gene: CHRNA3

Linked Data

• dbSNP Id: rs2053475083

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78617139_78617156dup , CM000677.2:g.78617139_78617156dup	GRCh38
NC_000015.9:g.78909481_78909498dup , CM000677.1:g.78909481_78909498dup	GRCh37
NC_000015.8:g.76696536_76696553dup	NCBI36
NG_016143.1:g.9142_9159dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.268-21_268-4dup MANE Select	ENSP00000315602.5:n.268-21_268-4dup
ENST00000326828.5:c.268-21_268-4dup	ENSP00000315602.5:n.268-21_268-4dup
ENST00000348639.7:c.268-21_268-4dup	ENSP00000267951.4:n.268-21_268-4dup
ENST00000559658.5:c.268-21_268-4dup	ENSP00000452896.1:n.268-21_268-4dup
NM_000743.4:c.268-21_268-4dup	NP_000734.2:n.268-21_268-4dup
NM_001166694.1:c.268-21_268-4dup	NP_001160166.1:n.268-21_268-4dup
NR_046313.1:n.769-21_769-4dup
XM_006720382.1:c.67-21_67-4dup	XP_006720445.1:n.67-21_67-4dup
XM_011521173.1:c.187-21_187-4dup	XP_011519475.1:n.187-21_187-4dup
XM_006720382.3:c.67-21_67-4dup	XP_006720445.1:n.67-21_67-4dup
NM_000743.5:c.268-21_268-4dup MANE Select	NP_000734.2:n.268-21_268-4dup
NM_001166694.2:c.268-21_268-4dup	NP_001160166.1:n.268-21_268-4dup
NR_046313.2:n.470-21_470-4dup