Canonical Allele Identifier: CA393585596

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78894350C>T (hg19) ; chr15:g.78602008C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602008C>T , CM000677.2:g.78602008C>T	GRCh38
NC_000015.9:g.78894350C>T , CM000677.1:g.78894350C>T	GRCh37
NC_000015.8:g.76681405C>T	NCBI36
NG_016143.1:g.24288G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.634G>A MANE Select	ENSP00000315602.5:p.Ala212Thr
ENST00000326828.5:c.634G>A	ENSP00000315602.5:p.Ala212Thr
ENST00000348639.7:c.634G>A	ENSP00000267951.4:p.Ala212Thr
ENST00000558903.1:n.341G>A
ENST00000559658.5:c.634G>A	ENSP00000452896.1:p.Ala212Thr
NM_000743.4:c.634G>A	NP_000734.2:p.Ala212Thr
NM_001166694.1:c.634G>A	NP_001160166.1:p.Ala212Thr
NR_046313.1:n.1135G>A
XM_006720382.1:c.433G>A	XP_006720445.1:p.Ala145Thr
XM_011521173.1:c.553G>A	XP_011519475.1:p.Ala185Thr
XM_006720382.3:c.433G>A	XP_006720445.1:p.Ala145Thr
NM_000743.5:c.634G>A MANE Select	NP_000734.2:p.Ala212Thr
NM_001166694.2:c.634G>A	NP_001160166.1:p.Ala212Thr
NR_046313.2:n.836G>A