Canonical Allele Identifier: CA393585018

Gene: CHRNA3

Linked Data

• dbSNP Id: rs2053207771
• gnomAD v3: 15-78601915-A-T
• gnomAD v4: 15-78601915-A-T
• MyVariant Identifiers: chr15:g.78894257A>T (hg19) ; chr15:g.78601915A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601915A>T , CM000677.2:g.78601915A>T	GRCh38
NC_000015.9:g.78894257A>T , CM000677.1:g.78894257A>T	GRCh37
NC_000015.8:g.76681312A>T	NCBI36
NG_016143.1:g.24381T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.727T>A MANE Select	ENSP00000315602.5:p.Phe243Ile
ENST00000326828.5:c.727T>A	ENSP00000315602.5:p.Phe243Ile
ENST00000348639.7:c.727T>A	ENSP00000267951.4:p.Phe243Ile
ENST00000558903.1:n.434T>A
ENST00000559658.5:c.727T>A	ENSP00000452896.1:p.Phe243Ile
NM_000743.4:c.727T>A	NP_000734.2:p.Phe243Ile
NM_001166694.1:c.727T>A	NP_001160166.1:p.Phe243Ile
NR_046313.1:n.1228T>A
XM_006720382.1:c.526T>A	XP_006720445.1:p.Phe176Ile
XM_011521173.1:c.646T>A	XP_011519475.1:p.Phe216Ile
XM_006720382.3:c.526T>A	XP_006720445.1:p.Phe176Ile
NM_000743.5:c.727T>A MANE Select	NP_000734.2:p.Phe243Ile
NM_001166694.2:c.727T>A	NP_001160166.1:p.Phe243Ile
NR_046313.2:n.929T>A