Canonical Allele Identifier: CA393585148

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78894284A>T (hg19) ; chr15:g.78601942A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601942A>T , CM000677.2:g.78601942A>T	GRCh38
NC_000015.9:g.78894284A>T , CM000677.1:g.78894284A>T	GRCh37
NC_000015.8:g.76681339A>T	NCBI36
NG_016143.1:g.24354T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.700T>A MANE Select	ENSP00000315602.5:p.Ser234Thr
ENST00000326828.5:c.700T>A	ENSP00000315602.5:p.Ser234Thr
ENST00000348639.7:c.700T>A	ENSP00000267951.4:p.Ser234Thr
ENST00000558903.1:n.407T>A
ENST00000559658.5:c.700T>A	ENSP00000452896.1:p.Ser234Thr
NM_000743.4:c.700T>A	NP_000734.2:p.Ser234Thr
NM_001166694.1:c.700T>A	NP_001160166.1:p.Ser234Thr
NR_046313.1:n.1201T>A
XM_006720382.1:c.499T>A	XP_006720445.1:p.Ser167Thr
XM_011521173.1:c.619T>A	XP_011519475.1:p.Ser207Thr
XM_006720382.3:c.499T>A	XP_006720445.1:p.Ser167Thr
NM_000743.5:c.700T>A MANE Select	NP_000734.2:p.Ser234Thr
NM_001166694.2:c.700T>A	NP_001160166.1:p.Ser234Thr
NR_046313.2:n.902T>A