Linked Data
ClinVar Variation Id:
218301
gnomAD v4:
9-133354959-T-C
MyVariant Identifiers:
chr9:g.133354959T>C (hg38)
PubMed:
PMID:24027061
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133354959T>C , CM000671.2:g.133354959T>C | GRCh38 |
| NC_000009.10:g.135211635T>C | NCBI36 |
| NG_008477.1:g.6548A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371974.8:c.107-2A>G MANE Select | ENSP00000361042.3:n.107-2A>G | |
| ENST00000371974.7:c.107-2A>G | ENSP00000361042.3:n.107-2A>G | |
| ENST00000437995.1:n.53-2A>G | ||
| ENST00000615505.4:c.-221-2A>G | ENSP00000482067.1:n.-221-2A>G | |
| NM_001280787.1:c.-221-2A>G | NP_001267716.1:n.-221-2A>G | |
| NM_003172.3:c.107-2A>G | NP_003163.1:n.107-2A>G | |
| XM_011518942.1:c.-221-2A>G | XP_011517244.1:n.-221-2A>G | |
| NM_003172.4:c.107-2A>G MANE Select | NP_003163.1:n.107-2A>G |