UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Linked Data
ClinVar Variation Id:
30510
dbSNP Id:
rs281875284
gnomAD v4:
20-58418289-C-T
PubMed:
PMID:20940299
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.58418289C>T , CM000682.2:g.58418289C>T | GRCh38 |
| NC_000020.10:g.56993345C>T , CM000682.1:g.56993345C>T | GRCh37 |
| NC_000020.9:g.56426751C>T | NCBI36 |
| NG_008073.2:g.34101C>T , LRG_656:g.34101C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000475243.6:c.137C>T MANE Select | ENSP00000417175.1:p.Thr46Ile | |
| ENST00000265619.6:n.435C>T | ||
| ENST00000395802.7:c.137C>T | ENSP00000379147.3:p.Thr46Ile | |
| ENST00000475243.5:c.137C>T | ENSP00000417175.1:p.Thr46Ile | |
| ENST00000520497.1:c.137C>T | ENSP00000430426.1:p.Thr46Ile | |
| NM_001195677.1:c.137C>T | NP_001182606.1:p.Thr46Ile | |
| NM_004738.4:c.137C>T , LRG_656t1:c.137C>T | NP_004729.1:p.Thr46Ile | |
| NR_036633.1:n.478C>T | ||
| XR_001754433.2:n.386C>T | ||
| NM_001195677.2:c.137C>T | NP_001182606.1:p.Thr46Ile | |
| NM_004738.5:c.137C>T MANE Select | NP_004729.1:p.Thr46Ile | |
| NR_036633.2:n.368C>T |