Linked Data
ClinVar Variation Id:
1629961
ClinVar RCV Id:
RCV002118710
dbSNP Id:
rs759299447
gnomAD v3:
22-46352138-C-T
gnomAD v4:
22-46352138-C-T
COSMIC:
COSM3555477
MyVariant Identifiers:
chr22:g.46748035C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.46352138C>T , CM000684.2:g.46352138C>T | GRCh38 |
| NC_000022.10:g.46748035C>T , CM000684.1:g.46748035C>T | GRCh37 |
| NC_000022.9:g.45126699C>T | NCBI36 |
| NG_012173.1:g.21738C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000465378.6:n.717C>T | ||
| ENST00000642923.1:c.564C>T | ENSP00000494255.1:p.Phe188= | |
| ENST00000643137.1:c.564C>T | ENSP00000495331.1:p.Phe188= | |
| ENST00000644006.1:c.*113C>T | ENSP00000493778.1:n.*113C>T | |
| ENST00000645026.1:n.720C>T | ||
| ENST00000645190.1:c.669C>T MANE Select | ENSP00000496496.1:p.Phe223= | |
| ENST00000647301.1:c.*113C>T | ENSP00000496641.1:n.*113C>T | |
| ENST00000290846.8:c.669C>T | ENSP00000290846.4:p.Phe223= | |
| ENST00000381019.3:c.669C>T | ENSP00000370407.3:p.Phe223= | |
| ENST00000381021.7:c.*262C>T | ENSP00000370409.3:n.*262C>T | |
| ENST00000441818.5:c.*203C>T | ENSP00000393014.1:n.*203C>T | |
| ENST00000453630.5:c.*207C>T | ENSP00000398488.1:n.*207C>T | |
| ENST00000456595.5:c.*203C>T | ENSP00000413880.1:n.*203C>T | |
| ENST00000457572.5:c.*113C>T | ENSP00000407700.1:n.*113C>T | |
| ENST00000463785.1:n.137C>T | ||
| ENST00000479648.1:n.489C>T | ||
| ENST00000485175.5:n.629C>T | ||
| ENST00000486620.5:n.711C>T | ||
| NM_001282782.1:c.327C>T | NP_001269711.1:p.Phe109= | |
| NM_001282783.1:c.249C>T | NP_001269712.1:p.Phe83= | |
| NM_001282784.1:c.249C>T | NP_001269713.1:p.Phe83= | |
| NM_001282785.1:c.669C>T | NP_001269714.1:p.Phe223= | |
| NM_018006.4:c.669C>T | NP_060476.2:p.Phe223= | |
| NR_104240.1:n.978C>T | ||
| NR_104241.1:n.871C>T | ||
| XM_005261678.1:c.273C>T | XP_005261735.1:p.Phe91= | |
| XM_005261681.1:c.273C>T | XP_005261738.1:p.Phe91= | |
| XM_011530271.1:c.564C>T | XP_011528573.1:p.Phe188= | |
| XM_011530272.1:c.669C>T | XP_011528574.1:p.Phe223= | |
| XM_011530273.1:c.669C>T | XP_011528575.1:p.Phe223= | |
| XM_011530274.1:c.327C>T | XP_011528576.1:p.Phe109= | |
| XM_011530275.1:c.273C>T | XP_011528577.1:p.Phe91= | |
| XM_011530271.2:c.564C>T | XP_011528573.1:p.Phe188= | |
| XM_011530272.2:c.669C>T | XP_011528574.1:p.Phe223= | |
| XM_011530273.2:c.669C>T | XP_011528575.1:p.Phe223= | |
| XM_011530274.2:c.327C>T | XP_011528576.1:p.Phe109= | |
| XM_024452260.1:c.564C>T | XP_024308028.1:p.Phe188= | |
| XR_001755261.2:n.715C>T | ||
| XR_001755262.2:n.715C>T | ||
| NM_018006.5:c.669C>T MANE Select | NP_060476.2:p.Phe223= | |
| NM_001282782.2:c.327C>T | NP_001269711.1:p.Phe109= | |
| NM_001282783.2:c.249C>T | NP_001269712.1:p.Phe83= | |
| NM_001282784.2:c.249C>T | NP_001269713.1:p.Phe83= | |
| NM_001282785.2:c.669C>T | NP_001269714.1:p.Phe223= | |
| NR_104240.2:n.665C>T | ||
| NR_104241.2:n.558C>T |