Canonical Allele Identifier: CA393585169

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78894287A>C (hg19) ; chr15:g.78601945A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601945A>C , CM000677.2:g.78601945A>C	GRCh38
NC_000015.9:g.78894287A>C , CM000677.1:g.78894287A>C	GRCh37
NC_000015.8:g.76681342A>C	NCBI36
NG_016143.1:g.24351T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.697T>G MANE Select	ENSP00000315602.5:p.Tyr233Asp
ENST00000326828.5:c.697T>G	ENSP00000315602.5:p.Tyr233Asp
ENST00000348639.7:c.697T>G	ENSP00000267951.4:p.Tyr233Asp
ENST00000558903.1:n.404T>G
ENST00000559658.5:c.697T>G	ENSP00000452896.1:p.Tyr233Asp
NM_000743.4:c.697T>G	NP_000734.2:p.Tyr233Asp
NM_001166694.1:c.697T>G	NP_001160166.1:p.Tyr233Asp
NR_046313.1:n.1198T>G
XM_006720382.1:c.496T>G	XP_006720445.1:p.Tyr166Asp
XM_011521173.1:c.616T>G	XP_011519475.1:p.Tyr206Asp
XM_006720382.3:c.496T>G	XP_006720445.1:p.Tyr166Asp
NM_000743.5:c.697T>G MANE Select	NP_000734.2:p.Tyr233Asp
NM_001166694.2:c.697T>G	NP_001160166.1:p.Tyr233Asp
NR_046313.2:n.899T>G