Linked Data
ClinVar Variation Id:
347685
ClinVar RCV Id:
RCV000383850
dbSNP Id:
rs886059121
gnomAD v2:
4-149000737-T-C
gnomAD v3:
4-148079586-T-C
gnomAD v4:
4-148079586-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.148079586T>C , CM000666.2:g.148079586T>C | GRCh38 |
| NC_000004.11:g.149000737T>C , CM000666.1:g.149000737T>C | GRCh37 |
| NC_000004.10:g.149220187T>C | NCBI36 |
| NG_013350.1:g.367936A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358102.8:c.*1758A>G MANE Select | ENSP00000350815.3:n.*1758A>G | |
| ENST00000344721.8:c.*1758A>G | ENSP00000341390.4:n.*1758A>G | |
| ENST00000358102.7:c.*1758A>G | ENSP00000350815.3:n.*1758A>G | |
| ENST00000625323.2:c.*1758A>G | ENSP00000486719.1:n.*1758A>G | |
| NM_000901.4:c.*1758A>G | NP_000892.2:n.*1758A>G | |
| NM_001166104.1:c.*1758A>G | NP_001159576.1:n.*1758A>G | |
| XM_011531975.1:c.*1758A>G | XP_011530277.1:n.*1758A>G | |
| XM_011531976.1:c.*1758A>G | XP_011530278.1:n.*1758A>G | |
| XM_011531977.1:c.*1758A>G | XP_011530279.1:n.*1758A>G | |
| NM_001354819.1:c.*1758A>G | NP_001341748.1:n.*1758A>G | |
| NR_148974.1:n.4580A>G | ||
| NM_000901.5:c.*1758A>G MANE Select | NP_000892.2:n.*1758A>G | |
| NM_001166104.2:c.*1758A>G | NP_001159576.1:n.*1758A>G | |
| NR_148974.2:n.4474A>G |