Canonical Allele Identifier: CA393586073

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78894498G>C (hg19) ; chr15:g.78602156G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602156G>C , CM000677.2:g.78602156G>C	GRCh38
NC_000015.9:g.78894498G>C , CM000677.1:g.78894498G>C	GRCh37
NC_000015.8:g.76681553G>C	NCBI36
NG_016143.1:g.24140C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.486C>G MANE Select	ENSP00000315602.5:p.Asp162Glu
ENST00000326828.5:c.486C>G	ENSP00000315602.5:p.Asp162Glu
ENST00000348639.7:c.486C>G	ENSP00000267951.4:p.Asp162Glu
ENST00000558903.1:n.193C>G
ENST00000559658.5:c.486C>G	ENSP00000452896.1:p.Asp162Glu
NM_000743.4:c.486C>G	NP_000734.2:p.Asp162Glu
NM_001166694.1:c.486C>G	NP_001160166.1:p.Asp162Glu
NR_046313.1:n.987C>G
XM_006720382.1:c.285C>G	XP_006720445.1:p.Asp95Glu
XM_011521173.1:c.405C>G	XP_011519475.1:p.Asp135Glu
XM_006720382.3:c.285C>G	XP_006720445.1:p.Asp95Glu
NM_000743.5:c.486C>G MANE Select	NP_000734.2:p.Asp162Glu
NM_001166694.2:c.486C>G	NP_001160166.1:p.Asp162Glu
NR_046313.2:n.688C>G