Canonical Allele Identifier: CA393584808

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78601872-A-C
• MyVariant Identifiers: chr15:g.78894214A>C (hg19) ; chr15:g.78601872A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601872A>C , CM000677.2:g.78601872A>C	GRCh38
NC_000015.9:g.78894214A>C , CM000677.1:g.78894214A>C	GRCh37
NC_000015.8:g.76681269A>C	NCBI36
NG_016143.1:g.24424T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.770T>G MANE Select	ENSP00000315602.5:p.Phe257Cys
ENST00000326828.5:c.770T>G	ENSP00000315602.5:p.Phe257Cys
ENST00000348639.7:c.770T>G	ENSP00000267951.4:p.Phe257Cys
ENST00000558903.1:n.477T>G
ENST00000559658.5:c.770T>G	ENSP00000452896.1:p.Phe257Cys
NM_000743.4:c.770T>G	NP_000734.2:p.Phe257Cys
NM_001166694.1:c.770T>G	NP_001160166.1:p.Phe257Cys
NR_046313.1:n.1271T>G
XM_006720382.1:c.569T>G	XP_006720445.1:p.Phe190Cys
XM_011521173.1:c.689T>G	XP_011519475.1:p.Phe230Cys
XM_006720382.3:c.569T>G	XP_006720445.1:p.Phe190Cys
NM_000743.5:c.770T>G MANE Select	NP_000734.2:p.Phe257Cys
NM_001166694.2:c.770T>G	NP_001160166.1:p.Phe257Cys
NR_046313.2:n.972T>G