Canonical Allele Identifier: CA491986602

Gene: CHRNA3

Linked Data

• gnomAD v3: 15-78601985-G-A
• gnomAD v4: 15-78601985-G-A
• MyVariant Identifiers: chr15:g.78894327G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601985G>A , CM000677.2:g.78601985G>A	GRCh38
NC_000015.9:g.78894327G>A , CM000677.1:g.78894327G>A	GRCh37
NC_000015.8:g.76681382G>A	NCBI36
NG_016143.1:g.24311C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.657C>T MANE Select	ENSP00000315602.5:p.Ile219=
ENST00000326828.5:c.657C>T	ENSP00000315602.5:p.Ile219=
ENST00000348639.7:c.657C>T	ENSP00000267951.4:p.Ile219=
ENST00000558903.1:n.364C>T
ENST00000559658.5:c.657C>T	ENSP00000452896.1:p.Ile219=
NM_000743.4:c.657C>T	NP_000734.2:p.Ile219=
NM_001166694.1:c.657C>T	NP_001160166.1:p.Ile219=
NR_046313.1:n.1158C>T
XM_006720382.1:c.456C>T	XP_006720445.1:p.Ile152=
XM_011521173.1:c.576C>T	XP_011519475.1:p.Ile192=
XM_006720382.3:c.456C>T	XP_006720445.1:p.Ile152=
NM_000743.5:c.657C>T MANE Select	NP_000734.2:p.Ile219=
NM_001166694.2:c.657C>T	NP_001160166.1:p.Ile219=
NR_046313.2:n.859C>T