Canonical Allele Identifier: CA491986527

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1242393663
• gnomAD v3: 15-78601892-G-A
• gnomAD v4: 15-78601892-G-A
• MyVariant Identifiers: chr15:g.78894234G>A (hg19) ; chr15:g.78601892G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601892G>A , CM000677.2:g.78601892G>A	GRCh38
NC_000015.9:g.78894234G>A , CM000677.1:g.78894234G>A	GRCh37
NC_000015.8:g.76681289G>A	NCBI36
NG_016143.1:g.24404C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.750C>T MANE Select	ENSP00000315602.5:p.Ile250=
ENST00000326828.5:c.750C>T	ENSP00000315602.5:p.Ile250=
ENST00000348639.7:c.750C>T	ENSP00000267951.4:p.Ile250=
ENST00000558903.1:n.457C>T
ENST00000559658.5:c.750C>T	ENSP00000452896.1:p.Ile250=
NM_000743.4:c.750C>T	NP_000734.2:p.Ile250=
NM_001166694.1:c.750C>T	NP_001160166.1:p.Ile250=
NR_046313.1:n.1251C>T
XM_006720382.1:c.549C>T	XP_006720445.1:p.Ile183=
XM_011521173.1:c.669C>T	XP_011519475.1:p.Ile223=
XM_006720382.3:c.549C>T	XP_006720445.1:p.Ile183=
NM_000743.5:c.750C>T MANE Select	NP_000734.2:p.Ile250=
NM_001166694.2:c.750C>T	NP_001160166.1:p.Ile250=
NR_046313.2:n.952C>T