Canonical Allele Identifier: CA491986321

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1485291314
• gnomAD v4: 15-78602018-G-A
• MyVariant Identifiers: chr15:g.78894360G>A (hg19) ; chr15:g.78602018G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602018G>A , CM000677.2:g.78602018G>A	GRCh38
NC_000015.9:g.78894360G>A , CM000677.1:g.78894360G>A	GRCh37
NC_000015.8:g.76681415G>A	NCBI36
NG_016143.1:g.24278C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.624C>T MANE Select	ENSP00000315602.5:p.Ala208=
ENST00000326828.5:c.624C>T	ENSP00000315602.5:p.Ala208=
ENST00000348639.7:c.624C>T	ENSP00000267951.4:p.Ala208=
ENST00000558903.1:n.331C>T
ENST00000559658.5:c.624C>T	ENSP00000452896.1:p.Ala208=
NM_000743.4:c.624C>T	NP_000734.2:p.Ala208=
NM_001166694.1:c.624C>T	NP_001160166.1:p.Ala208=
NR_046313.1:n.1125C>T
XM_006720382.1:c.423C>T	XP_006720445.1:p.Ala141=
XM_011521173.1:c.543C>T	XP_011519475.1:p.Ala181=
XM_006720382.3:c.423C>T	XP_006720445.1:p.Ala141=
NM_000743.5:c.624C>T MANE Select	NP_000734.2:p.Ala208=
NM_001166694.2:c.624C>T	NP_001160166.1:p.Ala208=
NR_046313.2:n.826C>T