Canonical Allele Identifier: CA491986539

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78602216-C-T
• MyVariant Identifiers: chr15:g.78894558C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602216C>T , CM000677.2:g.78602216C>T	GRCh38
NC_000015.9:g.78894558C>T , CM000677.1:g.78894558C>T	GRCh37
NC_000015.8:g.76681613C>T	NCBI36
NG_016143.1:g.24080G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.426G>A MANE Select	ENSP00000315602.5:p.Lys142=
ENST00000326828.5:c.426G>A	ENSP00000315602.5:p.Lys142=
ENST00000348639.7:c.426G>A	ENSP00000267951.4:p.Lys142=
ENST00000558903.1:n.133G>A
ENST00000559658.5:c.426G>A	ENSP00000452896.1:p.Lys142=
NM_000743.4:c.426G>A	NP_000734.2:p.Lys142=
NM_001166694.1:c.426G>A	NP_001160166.1:p.Lys142=
NR_046313.1:n.927G>A
XM_006720382.1:c.225G>A	XP_006720445.1:p.Lys75=
XM_011521173.1:c.345G>A	XP_011519475.1:p.Lys115=
XM_006720382.3:c.225G>A	XP_006720445.1:p.Lys75=
NM_000743.5:c.426G>A MANE Select	NP_000734.2:p.Lys142=
NM_001166694.2:c.426G>A	NP_001160166.1:p.Lys142=
NR_046313.2:n.628G>A