Canonical Allele Identifier: CA7684429

Gene: CHRNA3

Linked Data

• dbSNP Id: rs75253420
• ExAC: 15:78894349 G / A
• gnomAD v2: 15-78894349-G-A
• gnomAD v3: 15-78602007-G-A
• gnomAD v4: 15-78602007-G-A
• MyVariant Identifiers: chr15:g.78894349G>A (hg19) ; chr15:g.78602007G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602007G>A , CM000677.2:g.78602007G>A	GRCh38
NC_000015.9:g.78894349G>A , CM000677.1:g.78894349G>A	GRCh37
NC_000015.8:g.76681404G>A	NCBI36
NG_016143.1:g.24289C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.635C>T MANE Select	ENSP00000315602.5:p.Ala212Val
ENST00000326828.5:c.635C>T	ENSP00000315602.5:p.Ala212Val
ENST00000348639.7:c.635C>T	ENSP00000267951.4:p.Ala212Val
ENST00000558903.1:n.342C>T
ENST00000559658.5:c.635C>T	ENSP00000452896.1:p.Ala212Val
NM_000743.4:c.635C>T	NP_000734.2:p.Ala212Val
NM_001166694.1:c.635C>T	NP_001160166.1:p.Ala212Val
NR_046313.1:n.1136C>T
XM_006720382.1:c.434C>T	XP_006720445.1:p.Ala145Val
XM_011521173.1:c.554C>T	XP_011519475.1:p.Ala185Val
XM_006720382.3:c.434C>T	XP_006720445.1:p.Ala145Val
NM_000743.5:c.635C>T MANE Select	NP_000734.2:p.Ala212Val
NM_001166694.2:c.635C>T	NP_001160166.1:p.Ala212Val
NR_046313.2:n.837C>T