Canonical Allele Identifier: CA491986444

Gene: CHRNA3

Linked Data

• dbSNP Id: rs2053205245
• gnomAD v4: 15-78601826-C-T
• MyVariant Identifiers: chr15:g.78894168C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601826C>T , CM000677.2:g.78601826C>T	GRCh38
NC_000015.9:g.78894168C>T , CM000677.1:g.78894168C>T	GRCh37
NC_000015.8:g.76681223C>T	NCBI36
NG_016143.1:g.24470G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.816G>A MANE Select	ENSP00000315602.5:p.Lys272=
ENST00000326828.5:c.816G>A	ENSP00000315602.5:p.Lys272=
ENST00000348639.7:c.816G>A	ENSP00000267951.4:p.Lys272=
ENST00000558903.1:n.523G>A
ENST00000559658.5:c.816G>A	ENSP00000452896.1:p.Lys272=
NM_000743.4:c.816G>A	NP_000734.2:p.Lys272=
NM_001166694.1:c.816G>A	NP_001160166.1:p.Lys272=
NR_046313.1:n.1317G>A
XM_006720382.1:c.615G>A	XP_006720445.1:p.Lys205=
XM_011521173.1:c.735G>A	XP_011519475.1:p.Lys245=
XM_006720382.3:c.615G>A	XP_006720445.1:p.Lys205=
NM_000743.5:c.816G>A MANE Select	NP_000734.2:p.Lys272=
NM_001166694.2:c.816G>A	NP_001160166.1:p.Lys272=
NR_046313.2:n.1018G>A