Canonical Allele Identifier: CA715965016

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1168915527
• MyVariant Identifiers: chr15:g.78894868G>T (hg19) ; chr15:g.78602526G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602526G>T , CM000677.2:g.78602526G>T	GRCh38
NC_000015.9:g.78894868G>T , CM000677.1:g.78894868G>T	GRCh37
NC_000015.8:g.76681923G>T	NCBI36
NG_016143.1:g.23770C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.378-262C>A MANE Select	ENSP00000315602.5:n.378-262C>A
ENST00000326828.5:c.378-262C>A	ENSP00000315602.5:n.378-262C>A
ENST00000348639.7:c.378-262C>A	ENSP00000267951.4:n.378-262C>A
ENST00000558903.1:n.85-262C>A
ENST00000559658.5:c.378-262C>A	ENSP00000452896.1:n.378-262C>A
NM_000743.4:c.378-262C>A	NP_000734.2:n.378-262C>A
NM_001166694.1:c.378-262C>A	NP_001160166.1:n.378-262C>A
NR_046313.1:n.879-262C>A
XM_006720382.1:c.177-262C>A	XP_006720445.1:n.177-262C>A
XM_011521173.1:c.297-262C>A	XP_011519475.1:n.297-262C>A
XM_006720382.3:c.177-262C>A	XP_006720445.1:n.177-262C>A
NM_000743.5:c.378-262C>A MANE Select	NP_000734.2:n.378-262C>A
NM_001166694.2:c.378-262C>A	NP_001160166.1:n.378-262C>A
NR_046313.2:n.580-262C>A