Linked Data
ClinVar Variation Id:
403463
dbSNP Id:
rs202081954
ExAC:
11:6413290 C / G
gnomAD v2:
11-6413290-C-G
gnomAD v3:
11-6392060-C-G
gnomAD v4:
11-6392060-C-G
PubMed:
PMID:23891399
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6392060C>G , CM000673.2:g.6392060C>G | GRCh38 |
| NC_000011.9:g.6413290C>G , CM000673.1:g.6413290C>G | GRCh37 |
| NC_000011.8:g.6369866C>G | NCBI36 |
| NG_011780.1:g.6636C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342245.9:c.995C>G MANE Select | ENSP00000340409.4:p.Pro332Arg | |
| ENST00000342245.8:c.995C>G | ENSP00000340409.4:p.Pro332Arg | |
| ENST00000526280.1:c.184C>G | ||
| ENST00000527275.5:c.992C>G | ENSP00000435350.1:p.Pro331Arg | |
| ENST00000531303.5:c.438+557C>G | ENSP00000432625.1:n.438+557C>G | |
| ENST00000533123.5:c.995C>G | ENSP00000435950.1:p.Pro332Arg | |
| ENST00000534405.5:c.995C>G | ENSP00000434353.1:p.Pro332Arg | |
| NM_000543.4:c.995C>G | NP_000534.3:p.Pro332Arg | |
| NM_001007593.2:c.992C>G | NP_001007594.2:p.Pro331Arg | |
| XM_005253075.3:c.995C>G | XP_005253132.1:p.Pro332Arg | |
| XM_011520303.1:c.995C>G | XP_011518605.1:p.Pro332Arg | |
| XM_011520304.1:c.995C>G | XP_011518606.1:p.Pro332Arg | |
| XR_930886.1:n.1293C>G | ||
| NM_001318087.1:c.995C>G | NP_001305016.1:p.Pro332Arg | |
| NM_001318088.1:c.34C>G | NP_001305017.1:p.Pro12Ala | |
| NM_001365135.1:c.995C>G | NP_001352064.1:p.Pro332Arg | |
| NR_027400.2:n.1180C>G | ||
| NR_134502.1:n.623+557C>G | ||
| XM_011520304.2:c.995C>G | XP_011518606.1:p.Pro332Arg | |
| XR_001747940.2:n.1120C>G | ||
| XR_002957158.1:n.1120C>G | ||
| NM_000543.5:c.995C>G MANE Select | NP_000534.3:p.Pro332Arg | |
| NM_001007593.3:c.992C>G | NP_001007594.2:p.Pro331Arg | |
| NM_001318087.2:c.995C>G | NP_001305016.1:p.Pro332Arg | |
| NM_001318088.2:c.34C>G | NP_001305017.1:p.Pro12Ala | |
| NM_001365135.2:c.995C>G | NP_001352064.1:p.Pro332Arg | |
| NR_027400.3:n.1120C>G | ||
| NR_134502.2:n.563+557C>G |