Canonical Allele Identifier: CA7684431

Gene: CHRNA3

Linked Data

• dbSNP Id: rs200244272
• ExAC: 15:78894356 T / C
• gnomAD v2: 15-78894356-T-C
• gnomAD v4: 15-78602014-T-C
• MyVariant Identifiers: chr15:g.78894356T>C (hg19) ; chr15:g.78602014T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602014T>C , CM000677.2:g.78602014T>C	GRCh38
NC_000015.9:g.78894356T>C , CM000677.1:g.78894356T>C	GRCh37
NC_000015.8:g.76681411T>C	NCBI36
NG_016143.1:g.24282A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.628A>G MANE Select	ENSP00000315602.5:p.Ile210Val
ENST00000326828.5:c.628A>G	ENSP00000315602.5:p.Ile210Val
ENST00000348639.7:c.628A>G	ENSP00000267951.4:p.Ile210Val
ENST00000558903.1:n.335A>G
ENST00000559658.5:c.628A>G	ENSP00000452896.1:p.Ile210Val
NM_000743.4:c.628A>G	NP_000734.2:p.Ile210Val
NM_001166694.1:c.628A>G	NP_001160166.1:p.Ile210Val
NR_046313.1:n.1129A>G
XM_006720382.1:c.427A>G	XP_006720445.1:p.Ile143Val
XM_011521173.1:c.547A>G	XP_011519475.1:p.Ile183Val
XM_006720382.3:c.427A>G	XP_006720445.1:p.Ile143Val
NM_000743.5:c.628A>G MANE Select	NP_000734.2:p.Ile210Val
NM_001166694.2:c.628A>G	NP_001160166.1:p.Ile210Val
NR_046313.2:n.830A>G