Canonical Allele Identifier: CA393586522

Gene: CHRNA3

Linked Data

• dbSNP Id: rs754167059
• gnomAD v2: 15-78894555-G-T
• MyVariant Identifiers: chr15:g.78894555G>T (hg19) ; chr15:g.78602213G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602213G>T , CM000677.2:g.78602213G>T	GRCh38
NC_000015.9:g.78894555G>T , CM000677.1:g.78894555G>T	GRCh37
NC_000015.8:g.76681610G>T	NCBI36
NG_016143.1:g.24083C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.429C>A MANE Select	ENSP00000315602.5:p.Tyr143Ter
ENST00000326828.5:c.429C>A	ENSP00000315602.5:p.Tyr143Ter
ENST00000348639.7:c.429C>A	ENSP00000267951.4:p.Tyr143Ter
ENST00000558903.1:n.136C>A
ENST00000559658.5:c.429C>A	ENSP00000452896.1:p.Tyr143Ter
NM_000743.4:c.429C>A	NP_000734.2:p.Tyr143Ter
NM_001166694.1:c.429C>A	NP_001160166.1:p.Tyr143Ter
NR_046313.1:n.930C>A
XM_006720382.1:c.228C>A	XP_006720445.1:p.Tyr76Ter
XM_011521173.1:c.348C>A	XP_011519475.1:p.Tyr116Ter
XM_006720382.3:c.228C>A	XP_006720445.1:p.Tyr76Ter
NM_000743.5:c.429C>A MANE Select	NP_000734.2:p.Tyr143Ter
NM_001166694.2:c.429C>A	NP_001160166.1:p.Tyr143Ter
NR_046313.2:n.631C>A