Canonical Allele Identifier: CA393584663

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78601815-C-T
• MyVariant Identifiers: chr15:g.78894157C>T (hg19) ; chr15:g.78601815C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601815C>T , CM000677.2:g.78601815C>T	GRCh38
NC_000015.9:g.78894157C>T , CM000677.1:g.78894157C>T	GRCh37
NC_000015.8:g.76681212C>T	NCBI36
NG_016143.1:g.24481G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.827G>A MANE Select	ENSP00000315602.5:p.Cys276Tyr
ENST00000326828.5:c.827G>A	ENSP00000315602.5:p.Cys276Tyr
ENST00000348639.7:c.827G>A	ENSP00000267951.4:p.Cys276Tyr
ENST00000558903.1:n.534G>A
ENST00000559658.5:c.827G>A	ENSP00000452896.1:p.Cys276Tyr
NM_000743.4:c.827G>A	NP_000734.2:p.Cys276Tyr
NM_001166694.1:c.827G>A	NP_001160166.1:p.Cys276Tyr
NR_046313.1:n.1328G>A
XM_006720382.1:c.626G>A	XP_006720445.1:p.Cys209Tyr
XM_011521173.1:c.746G>A	XP_011519475.1:p.Cys249Tyr
XM_006720382.3:c.626G>A	XP_006720445.1:p.Cys209Tyr
NM_000743.5:c.827G>A MANE Select	NP_000734.2:p.Cys276Tyr
NM_001166694.2:c.827G>A	NP_001160166.1:p.Cys276Tyr
NR_046313.2:n.1029G>A