Canonical Allele Identifier: CA393584723

Gene: CHRNA3

Linked Data

• dbSNP Id: rs2053205900
• gnomAD v3: 15-78601845-G-A
• gnomAD v4: 15-78601845-G-A
• MyVariant Identifiers: chr15:g.78894187G>A (hg19) ; chr15:g.78601845G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601845G>A , CM000677.2:g.78601845G>A	GRCh38
NC_000015.9:g.78894187G>A , CM000677.1:g.78894187G>A	GRCh37
NC_000015.8:g.76681242G>A	NCBI36
NG_016143.1:g.24451C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.797C>T MANE Select	ENSP00000315602.5:p.Pro266Leu
ENST00000326828.5:c.797C>T	ENSP00000315602.5:p.Pro266Leu
ENST00000348639.7:c.797C>T	ENSP00000267951.4:p.Pro266Leu
ENST00000558903.1:n.504C>T
ENST00000559658.5:c.797C>T	ENSP00000452896.1:p.Pro266Leu
NM_000743.4:c.797C>T	NP_000734.2:p.Pro266Leu
NM_001166694.1:c.797C>T	NP_001160166.1:p.Pro266Leu
NR_046313.1:n.1298C>T
XM_006720382.1:c.596C>T	XP_006720445.1:p.Pro199Leu
XM_011521173.1:c.716C>T	XP_011519475.1:p.Pro239Leu
XM_006720382.3:c.596C>T	XP_006720445.1:p.Pro199Leu
NM_000743.5:c.797C>T MANE Select	NP_000734.2:p.Pro266Leu
NM_001166694.2:c.797C>T	NP_001160166.1:p.Pro266Leu
NR_046313.2:n.999C>T