Canonical Allele Identifier: CA393586399

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78602195-C-G
• MyVariant Identifiers: chr15:g.78894537C>G (hg19) ; chr15:g.78602195C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602195C>G , CM000677.2:g.78602195C>G	GRCh38
NC_000015.9:g.78894537C>G , CM000677.1:g.78894537C>G	GRCh37
NC_000015.8:g.76681592C>G	NCBI36
NG_016143.1:g.24101G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.447G>C MANE Select	ENSP00000315602.5:p.Trp149Cys
ENST00000326828.5:c.447G>C	ENSP00000315602.5:p.Trp149Cys
ENST00000348639.7:c.447G>C	ENSP00000267951.4:p.Trp149Cys
ENST00000558903.1:n.154G>C
ENST00000559658.5:c.447G>C	ENSP00000452896.1:p.Trp149Cys
NM_000743.4:c.447G>C	NP_000734.2:p.Trp149Cys
NM_001166694.1:c.447G>C	NP_001160166.1:p.Trp149Cys
NR_046313.1:n.948G>C
XM_006720382.1:c.246G>C	XP_006720445.1:p.Trp82Cys
XM_011521173.1:c.366G>C	XP_011519475.1:p.Trp122Cys
XM_006720382.3:c.246G>C	XP_006720445.1:p.Trp82Cys
NM_000743.5:c.447G>C MANE Select	NP_000734.2:p.Trp149Cys
NM_001166694.2:c.447G>C	NP_001160166.1:p.Trp149Cys
NR_046313.2:n.649G>C