Canonical Allele Identifier: CA7684393

Gene: CHRNA3

Linked Data

• dbSNP Id: rs754395587
• ExAC: 15:78894133 G / A
• gnomAD v2: 15-78894133-G-A
• gnomAD v4: 15-78601791-G-A
• COSMIC: COSM2011188
• MyVariant Identifiers: chr15:g.78894133G>A (hg19) ; chr15:g.78601791G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601791G>A , CM000677.2:g.78601791G>A	GRCh38
NC_000015.9:g.78894133G>A , CM000677.1:g.78894133G>A	GRCh37
NC_000015.8:g.76681188G>A	NCBI36
NG_016143.1:g.24505C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.851C>T MANE Select	ENSP00000315602.5:p.Thr284Met
ENST00000326828.5:c.851C>T	ENSP00000315602.5:p.Thr284Met
ENST00000348639.7:c.851C>T	ENSP00000267951.4:p.Thr284Met
ENST00000558903.1:n.558C>T
ENST00000559658.5:c.851C>T	ENSP00000452896.1:p.Thr284Met
NM_000743.4:c.851C>T	NP_000734.2:p.Thr284Met
NM_001166694.1:c.851C>T	NP_001160166.1:p.Thr284Met
NR_046313.1:n.1352C>T
XM_006720382.1:c.650C>T	XP_006720445.1:p.Thr217Met
XM_011521173.1:c.770C>T	XP_011519475.1:p.Thr257Met
XM_006720382.3:c.650C>T	XP_006720445.1:p.Thr217Met
NM_000743.5:c.851C>T MANE Select	NP_000734.2:p.Thr284Met
NM_001166694.2:c.851C>T	NP_001160166.1:p.Thr284Met
NR_046313.2:n.1053C>T