Canonical Allele Identifier: CA273905732

Gene: CHRNA3

Linked Data

• dbSNP Id: rs76821682
• gnomAD v3: 15-78601994-T-G
• gnomAD v4: 15-78601994-T-G
• MyVariant Identifiers: chr15:g.78894336T>G (hg19) ; chr15:g.78601994T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601994T>G , CM000677.2:g.78601994T>G	GRCh38
NC_000015.9:g.78894336T>G , CM000677.1:g.78894336T>G	GRCh37
NC_000015.8:g.76681391T>G	NCBI36
NG_016143.1:g.24302A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.648A>C MANE Select	ENSP00000315602.5:p.Lys216Asn
ENST00000326828.5:c.648A>C	ENSP00000315602.5:p.Lys216Asn
ENST00000348639.7:c.648A>C	ENSP00000267951.4:p.Lys216Asn
ENST00000558903.1:n.355A>C
ENST00000559658.5:c.648A>C	ENSP00000452896.1:p.Lys216Asn
NM_000743.4:c.648A>C	NP_000734.2:p.Lys216Asn
NM_001166694.1:c.648A>C	NP_001160166.1:p.Lys216Asn
NR_046313.1:n.1149A>C
XM_006720382.1:c.447A>C	XP_006720445.1:p.Lys149Asn
XM_011521173.1:c.567A>C	XP_011519475.1:p.Lys189Asn
XM_006720382.3:c.447A>C	XP_006720445.1:p.Lys149Asn
NM_000743.5:c.648A>C MANE Select	NP_000734.2:p.Lys216Asn
NM_001166694.2:c.648A>C	NP_001160166.1:p.Lys216Asn
NR_046313.2:n.850A>C