Canonical Allele Identifier: CA491986541
Gene: CHRNA3 HGNC NCBI

Linked Data

dbSNP Id: rs2053207553
MyVariant Identifiers: chr15:g.78894246G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78601904G>T , CM000677.2:g.78601904G>T GRCh38
NC_000015.9:g.78894246G>T , CM000677.1:g.78894246G>T GRCh37
NC_000015.8:g.76681301G>T NCBI36
NG_016143.1:g.24392C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000326828.6:c.738C>A MANE Select ENSP00000315602.5:p.Ile246=
ENST00000326828.5:c.738C>A ENSP00000315602.5:p.Ile246=
ENST00000348639.7:c.738C>A ENSP00000267951.4:p.Ile246=
ENST00000558903.1:n.445C>A
ENST00000559658.5:c.738C>A ENSP00000452896.1:p.Ile246=
NM_000743.4:c.738C>A NP_000734.2:p.Ile246=
NM_001166694.1:c.738C>A NP_001160166.1:p.Ile246=
NR_046313.1:n.1239C>A
XM_006720382.1:c.537C>A XP_006720445.1:p.Ile179=
XM_011521173.1:c.657C>A XP_011519475.1:p.Ile219=
XM_006720382.3:c.537C>A XP_006720445.1:p.Ile179=
NM_000743.5:c.738C>A MANE Select NP_000734.2:p.Ile246=
NM_001166694.2:c.738C>A NP_001160166.1:p.Ile246=
NR_046313.2:n.940C>A