Canonical Allele Identifier: CA393584725

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78894187G>T (hg19) ; chr15:g.78601845G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.797C>A MANE Select	ENSP00000315602.5:p.Pro266His
ENST00000326828.5:c.797C>A	ENSP00000315602.5:p.Pro266His
ENST00000348639.7:c.797C>A	ENSP00000267951.4:p.Pro266His
ENST00000558903.1:n.504C>A
ENST00000559658.5:c.797C>A	ENSP00000452896.1:p.Pro266His
NM_000743.4:c.797C>A	NP_000734.2:p.Pro266His
NM_001166694.1:c.797C>A	NP_001160166.1:p.Pro266His
NR_046313.1:n.1298C>A
XM_006720382.1:c.596C>A	XP_006720445.1:p.Pro199His
XM_011521173.1:c.716C>A	XP_011519475.1:p.Pro239His
XM_006720382.3:c.596C>A	XP_006720445.1:p.Pro199His
NM_000743.5:c.797C>A MANE Select	NP_000734.2:p.Pro266His
NM_001166694.2:c.797C>A	NP_001160166.1:p.Pro266His
NR_046313.2:n.999C>A