Canonical Allele Identifier: CA7684432

Gene: CHRNA3

Linked Data

• ClinVar Variation Id: 779448
• ClinVar RCV Id: RCV000960286
• dbSNP Id: rs55958820
• ExAC: 15:78894357 G / T
• gnomAD v2: 15-78894357-G-T
• gnomAD v3: 15-78602015-G-T
• gnomAD v4: 15-78602015-G-T
• MyVariant Identifiers: chr15:g.78894357G>T (hg19) ; chr15:g.78602015G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602015G>T , CM000677.2:g.78602015G>T	GRCh38
NC_000015.9:g.78894357G>T , CM000677.1:g.78894357G>T	GRCh37
NC_000015.8:g.76681412G>T	NCBI36
NG_016143.1:g.24281C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.627C>A MANE Select	ENSP00000315602.5:p.Ile209=
ENST00000326828.5:c.627C>A	ENSP00000315602.5:p.Ile209=
ENST00000348639.7:c.627C>A	ENSP00000267951.4:p.Ile209=
ENST00000558903.1:n.334C>A
ENST00000559658.5:c.627C>A	ENSP00000452896.1:p.Ile209=
NM_000743.4:c.627C>A	NP_000734.2:p.Ile209=
NM_001166694.1:c.627C>A	NP_001160166.1:p.Ile209=
NR_046313.1:n.1128C>A
XM_006720382.1:c.426C>A	XP_006720445.1:p.Ile142=
XM_011521173.1:c.546C>A	XP_011519475.1:p.Ile182=
XM_006720382.3:c.426C>A	XP_006720445.1:p.Ile142=
NM_000743.5:c.627C>A MANE Select	NP_000734.2:p.Ile209=
NM_001166694.2:c.627C>A	NP_001160166.1:p.Ile209=
NR_046313.2:n.829C>A