Canonical Allele Identifier: CA393584766

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78894202A>C (hg19) ; chr15:g.78601860A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601860A>C , CM000677.2:g.78601860A>C	GRCh38
NC_000015.9:g.78894202A>C , CM000677.1:g.78894202A>C	GRCh37
NC_000015.8:g.76681257A>C	NCBI36
NG_016143.1:g.24436T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.782T>G MANE Select	ENSP00000315602.5:p.Leu261Arg
ENST00000326828.5:c.782T>G	ENSP00000315602.5:p.Leu261Arg
ENST00000348639.7:c.782T>G	ENSP00000267951.4:p.Leu261Arg
ENST00000558903.1:n.489T>G
ENST00000559658.5:c.782T>G	ENSP00000452896.1:p.Leu261Arg
NM_000743.4:c.782T>G	NP_000734.2:p.Leu261Arg
NM_001166694.1:c.782T>G	NP_001160166.1:p.Leu261Arg
NR_046313.1:n.1283T>G
XM_006720382.1:c.581T>G	XP_006720445.1:p.Leu194Arg
XM_011521173.1:c.701T>G	XP_011519475.1:p.Leu234Arg
XM_006720382.3:c.581T>G	XP_006720445.1:p.Leu194Arg
NM_000743.5:c.782T>G MANE Select	NP_000734.2:p.Leu261Arg
NM_001166694.2:c.782T>G	NP_001160166.1:p.Leu261Arg
NR_046313.2:n.984T>G