Canonical Allele Identifier: CA393585467

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78894323A>C (hg19) ; chr15:g.78601981A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601981A>C , CM000677.2:g.78601981A>C	GRCh38
NC_000015.9:g.78894323A>C , CM000677.1:g.78894323A>C	GRCh37
NC_000015.8:g.76681378A>C	NCBI36
NG_016143.1:g.24315T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.661T>G MANE Select	ENSP00000315602.5:p.Tyr221Asp
ENST00000326828.5:c.661T>G	ENSP00000315602.5:p.Tyr221Asp
ENST00000348639.7:c.661T>G	ENSP00000267951.4:p.Tyr221Asp
ENST00000558903.1:n.368T>G
ENST00000559658.5:c.661T>G	ENSP00000452896.1:p.Tyr221Asp
NM_000743.4:c.661T>G	NP_000734.2:p.Tyr221Asp
NM_001166694.1:c.661T>G	NP_001160166.1:p.Tyr221Asp
NR_046313.1:n.1162T>G
XM_006720382.1:c.460T>G	XP_006720445.1:p.Tyr154Asp
XM_011521173.1:c.580T>G	XP_011519475.1:p.Tyr194Asp
XM_006720382.3:c.460T>G	XP_006720445.1:p.Tyr154Asp
NM_000743.5:c.661T>G MANE Select	NP_000734.2:p.Tyr221Asp
NM_001166694.2:c.661T>G	NP_001160166.1:p.Tyr221Asp
NR_046313.2:n.863T>G