Canonical Allele Identifier: CA491986558

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1567077933
• gnomAD v4: 15-78602231-G-C
• MyVariant Identifiers: chr15:g.78894573G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602231G>C , CM000677.2:g.78602231G>C	GRCh38
NC_000015.9:g.78894573G>C , CM000677.1:g.78894573G>C	GRCh37
NC_000015.8:g.76681628G>C	NCBI36
NG_016143.1:g.24065C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.411C>G MANE Select	ENSP00000315602.5:p.Thr137=
ENST00000326828.5:c.411C>G	ENSP00000315602.5:p.Thr137=
ENST00000348639.7:c.411C>G	ENSP00000267951.4:p.Thr137=
ENST00000558903.1:n.118C>G
ENST00000559658.5:c.411C>G	ENSP00000452896.1:p.Thr137=
NM_000743.4:c.411C>G	NP_000734.2:p.Thr137=
NM_001166694.1:c.411C>G	NP_001160166.1:p.Thr137=
NR_046313.1:n.912C>G
XM_006720382.1:c.210C>G	XP_006720445.1:p.Thr70=
XM_011521173.1:c.330C>G	XP_011519475.1:p.Thr110=
XM_006720382.3:c.210C>G	XP_006720445.1:p.Thr70=
NM_000743.5:c.411C>G MANE Select	NP_000734.2:p.Thr137=
NM_001166694.2:c.411C>G	NP_001160166.1:p.Thr137=
NR_046313.2:n.613C>G