Linked Data
ClinVar Variation Id:
1119281
ClinVar RCV Id:
RCV001448659
dbSNP Id:
rs2124844869
gnomAD v4:
3-4376321-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.4376321A>G , CM000665.2:g.4376321A>G | GRCh38 |
| NC_000003.11:g.4418005A>G , CM000665.1:g.4418005A>G | GRCh37 |
| NC_000003.10:g.4393005A>G | NCBI36 |
| NG_016225.1:g.95962T>C | |
| NG_016225.2:g.95962T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272902.10:c.1014+9T>C MANE Select | ENSP00000272902.5:n.1014+9T>C | |
| ENST00000272902.9:c.1014+9T>C | ENSP00000272902.5:n.1014+9T>C | |
| ENST00000383843.9:c.939+9T>C | ENSP00000373355.5:n.939+9T>C | |
| ENST00000405420.2:c.955-14067T>C | ENSP00000384977.2:n.955-14067T>C | |
| ENST00000448413.5:c.1014+9T>C | ENSP00000404384.1:n.1014+9T>C | |
| ENST00000458465.6:c.618+9T>C | ENSP00000410060.2:n.618+9T>C | |
| NM_001164674.1:c.939+9T>C | NP_001158146.1:n.939+9T>C | |
| NM_001164675.1:c.955-14067T>C | NP_001158147.1:n.955-14067T>C | |
| NM_182760.3:c.1014+9T>C | NP_877437.2:n.1014+9T>C | |
| XM_011533623.1:c.1014+9T>C | XP_011531925.1:n.1014+9T>C | |
| XM_011533624.1:c.1014+9T>C | XP_011531926.1:n.1014+9T>C | |
| XM_011533625.1:c.1014+9T>C | XP_011531927.1:n.1014+9T>C | |
| XM_011533626.1:c.1014+9T>C | XP_011531928.1:n.1014+9T>C | |
| XM_011533624.3:c.1014+9T>C | XP_011531926.1:n.1014+9T>C | |
| XM_011533625.3:c.1014+9T>C | XP_011531927.1:n.1014+9T>C | |
| XM_011533626.3:c.1014+9T>C | XP_011531928.1:n.1014+9T>C | |
| XM_017006252.2:c.954+34544T>C | XP_016861741.1:n.954+34544T>C | |
| XM_017006253.1:c.939+9T>C | XP_016861742.1:n.939+9T>C | |
| XM_017006254.2:c.1014+9T>C | XP_016861743.1:n.1014+9T>C | |
| XM_017006255.2:c.1014+9T>C | XP_016861744.1:n.1014+9T>C | |
| NM_182760.4:c.1014+9T>C MANE Select | NP_877437.2:n.1014+9T>C | |
| NM_001164674.2:c.939+9T>C | NP_001158146.1:n.939+9T>C | |
| NM_001164675.2:c.955-14067T>C | NP_001158147.1:n.955-14067T>C |