Linked Data
ClinVar Variation Id:
2676
ClinVar RCV Id:
RCV000002795
dbSNP Id:
rs137852853
PubMed:
PMID:12757706
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.4362227C>G , CM000665.2:g.4362227C>G | GRCh38 |
| NC_000003.11:g.4403911C>G , CM000665.1:g.4403911C>G | GRCh37 |
| NC_000003.10:g.4378911C>G | NCBI36 |
| NG_016225.1:g.110056G>C | |
| NG_016225.2:g.110056G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272902.10:c.1042G>C MANE Select | ENSP00000272902.5:p.Ala348Pro | |
| ENST00000272902.9:c.1042G>C | ENSP00000272902.5:p.Ala348Pro | |
| ENST00000383843.9:c.967G>C | ENSP00000373355.5:p.Ala323Pro | |
| ENST00000405420.2:c.982G>C | ENSP00000384977.2:p.Ala328Pro | |
| ENST00000448413.5:c.1014+14103G>C | ENSP00000404384.1:n.1014+14103G>C | |
| ENST00000458465.6:c.646G>C | ENSP00000410060.2:p.Ala216Pro | |
| NM_001164674.1:c.967G>C | NP_001158146.1:p.Ala323Pro | |
| NM_001164675.1:c.982G>C | NP_001158147.1:p.Ala328Pro | |
| NM_182760.3:c.1042G>C | NP_877437.2:p.Ala348Pro | |
| XM_011533623.1:c.1014+14103G>C | XP_011531925.1:n.1014+14103G>C | |
| XM_011533624.1:c.1014+14103G>C | XP_011531926.1:n.1014+14103G>C | |
| XM_011533625.1:c.1014+14103G>C | XP_011531927.1:n.1014+14103G>C | |
| XM_011533626.1:c.1015-10596G>C | XP_011531928.1:n.1015-10596G>C | |
| XM_011533624.3:c.1014+14103G>C | XP_011531926.1:n.1014+14103G>C | |
| XM_011533625.3:c.1014+14103G>C | XP_011531927.1:n.1014+14103G>C | |
| XM_011533626.3:c.1015-10596G>C | XP_011531928.1:n.1015-10596G>C | |
| XM_017006252.2:c.954+48638G>C | XP_016861741.1:n.954+48638G>C | |
| XM_017006253.1:c.939+14103G>C | XP_016861742.1:n.939+14103G>C | |
| XM_017006254.2:c.1014+14103G>C | XP_016861743.1:n.1014+14103G>C | |
| XM_017006255.2:c.1014+14103G>C | XP_016861744.1:n.1014+14103G>C | |
| NM_182760.4:c.1042G>C MANE Select | NP_877437.2:p.Ala348Pro | |
| NM_001164674.2:c.967G>C | NP_001158146.1:p.Ala323Pro | |
| NM_001164675.2:c.982G>C | NP_001158147.1:p.Ala328Pro |