Canonical Allele Identifier: CA7684397

Gene: CHRNA3

Linked Data

• dbSNP Id: rs368207734
• ExAC: 15:78894176 C / A
• gnomAD v2: 15-78894176-C-A
• gnomAD v4: 15-78601834-C-A
• MyVariant Identifiers: chr15:g.78894176C>A (hg19) ; chr15:g.78601834C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601834C>A , CM000677.2:g.78601834C>A	GRCh38
NC_000015.9:g.78894176C>A , CM000677.1:g.78894176C>A	GRCh37
NC_000015.8:g.76681231C>A	NCBI36
NG_016143.1:g.24462G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.808G>T MANE Select	ENSP00000315602.5:p.Gly270Cys
ENST00000326828.5:c.808G>T	ENSP00000315602.5:p.Gly270Cys
ENST00000348639.7:c.808G>T	ENSP00000267951.4:p.Gly270Cys
ENST00000558903.1:n.515G>T
ENST00000559658.5:c.808G>T	ENSP00000452896.1:p.Gly270Cys
NM_000743.4:c.808G>T	NP_000734.2:p.Gly270Cys
NM_001166694.1:c.808G>T	NP_001160166.1:p.Gly270Cys
NR_046313.1:n.1309G>T
XM_006720382.1:c.607G>T	XP_006720445.1:p.Gly203Cys
XM_011521173.1:c.727G>T	XP_011519475.1:p.Gly243Cys
XM_006720382.3:c.607G>T	XP_006720445.1:p.Gly203Cys
NM_000743.5:c.808G>T MANE Select	NP_000734.2:p.Gly270Cys
NM_001166694.2:c.808G>T	NP_001160166.1:p.Gly270Cys
NR_046313.2:n.1010G>T