Canonical Allele Identifier: CA152387
Gene: CHRNA4 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 128750
dbSNP Id: rs1044394

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350733A>G , CM000682.2:g.63350733A>G GRCh38
NC_000020.10:g.61982085A>G , CM000682.1:g.61982085A>G GRCh37
NC_000020.9:g.61452529A>G NCBI36
NG_011931.1:g.15611T>C

Transcript Alleles

HGVS Amino-acid change
NM_000744.6:c.678T>C VV NP_000735.1:p.Cys226=
NM_001256573.1:c.150T>C VV NP_001243502.1:p.Cys50=
NR_046317.1:n.934T>C
XM_011528524.1:c.465T>C XP_011526826.1:p.Cys155=
XM_017027625.2:c.150T>C XP_016883114.1:p.Cys50=
XM_024451822.1:c.150T>C XP_024307590.1:p.Cys50=
ENST00000370263.8:c.678T>C ENSP00000359285.4:p.Cys226=
ENST00000463705.5:n.1326T>C
ENST00000467563.3:n.748T>C
ENST00000498043.6:n.702T>C
ENST00000615287.4:c.465T>C ENSP00000483388.1:p.Cys155=
ENST00000627000.1:c.*367T>C ENSP00000486914.1:p.=
ENST00000630240.1:n.399T>C