Canonical Allele Identifier: CA393584713

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78894181T>A (hg19) ; chr15:g.78601839T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601839T>A , CM000677.2:g.78601839T>A	GRCh38
NC_000015.9:g.78894181T>A , CM000677.1:g.78894181T>A	GRCh37
NC_000015.8:g.76681236T>A	NCBI36
NG_016143.1:g.24457A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.803A>T MANE Select	ENSP00000315602.5:p.Asp268Val
ENST00000326828.5:c.803A>T	ENSP00000315602.5:p.Asp268Val
ENST00000348639.7:c.803A>T	ENSP00000267951.4:p.Asp268Val
ENST00000558903.1:n.510A>T
ENST00000559658.5:c.803A>T	ENSP00000452896.1:p.Asp268Val
NM_000743.4:c.803A>T	NP_000734.2:p.Asp268Val
NM_001166694.1:c.803A>T	NP_001160166.1:p.Asp268Val
NR_046313.1:n.1304A>T
XM_006720382.1:c.602A>T	XP_006720445.1:p.Asp201Val
XM_011521173.1:c.722A>T	XP_011519475.1:p.Asp241Val
XM_006720382.3:c.602A>T	XP_006720445.1:p.Asp201Val
NM_000743.5:c.803A>T MANE Select	NP_000734.2:p.Asp268Val
NM_001166694.2:c.803A>T	NP_001160166.1:p.Asp268Val
NR_046313.2:n.1005A>T