Canonical Allele Identifier: CA393584956

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78894244T>G (hg19) ; chr15:g.78601902T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601902T>G , CM000677.2:g.78601902T>G	GRCh38
NC_000015.9:g.78894244T>G , CM000677.1:g.78894244T>G	GRCh37
NC_000015.8:g.76681299T>G	NCBI36
NG_016143.1:g.24394A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.740A>C MANE Select	ENSP00000315602.5:p.Asn247Thr
ENST00000326828.5:c.740A>C	ENSP00000315602.5:p.Asn247Thr
ENST00000348639.7:c.740A>C	ENSP00000267951.4:p.Asn247Thr
ENST00000558903.1:n.447A>C
ENST00000559658.5:c.740A>C	ENSP00000452896.1:p.Asn247Thr
NM_000743.4:c.740A>C	NP_000734.2:p.Asn247Thr
NM_001166694.1:c.740A>C	NP_001160166.1:p.Asn247Thr
NR_046313.1:n.1241A>C
XM_006720382.1:c.539A>C	XP_006720445.1:p.Asn180Thr
XM_011521173.1:c.659A>C	XP_011519475.1:p.Asn220Thr
XM_006720382.3:c.539A>C	XP_006720445.1:p.Asn180Thr
NM_000743.5:c.740A>C MANE Select	NP_000734.2:p.Asn247Thr
NM_001166694.2:c.740A>C	NP_001160166.1:p.Asn247Thr
NR_046313.2:n.942A>C