WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
Linked Data
ClinVar Variation Id:
227176
dbSNP Id:
rs41314453
gnomAD v3:
9-133442704-C-T
gnomAD v4:
9-133442704-C-T
MyVariant Identifiers:
chr9:g.133442704C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133442704C>T , CM000671.2:g.133442704C>T | GRCh38 |
| NC_000009.10:g.135297646C>T | NCBI36 |
| NG_011934.2:g.33366C>T , LRG_544:g.33366C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000355699.7:c.2195C>T MANE Select | ENSP00000347927.2:p.Ala732Val | |
| ENST00000355699.6:c.2195C>T | ENSP00000347927.2:p.Ala732Val | |
| ENST00000356589.6:c.2102C>T | ENSP00000348997.2:p.Ala701Val | |
| ENST00000371916.5:c.1225-2159C>T | ENSP00000360984.2:n.1225-2159C>T | |
| ENST00000371929.7:c.2195C>T | ENSP00000360997.3:p.Ala732Val | |
| ENST00000474918.1:c.*773-672C>T | ENSP00000435305.1:n.*773-672C>T | |
| ENST00000485925.5:n.1237-2159C>T | ||
| ENST00000495234.5:c.*1253-2159C>T | ENSP00000435274.1:n.*1253-2159C>T | |
| NM_139025.4:c.2195C>T , LRG_544t1:c.2195C>T | NP_620594.1:p.Ala732Val | |
| NM_139026.4:c.2102C>T | NP_620595.1:p.Ala701Val | |
| NM_139027.4:c.2195C>T | NP_620596.2:p.Ala732Val | |
| NR_024514.2:n.1256-2159C>T | ||
| XM_011518174.1:c.1805C>T | XP_011516476.1:p.Ala602Val | |
| XM_011518175.1:c.2195C>T | XP_011516477.1:p.Ala732Val | |
| XM_011518176.1:c.1211C>T | XP_011516478.1:p.Ala404Val | |
| XM_011518177.1:c.1205C>T | XP_011516479.1:p.Ala402Val | |
| XM_011518178.1:c.860C>T | XP_011516480.1:p.Ala287Val | |
| XM_011518179.1:c.860C>T | XP_011516481.1:p.Ala287Val | |
| XM_011518180.1:c.687-2159C>T | XP_011516482.1:n.687-2159C>T | |
| XM_011518176.3:c.1211C>T | XP_011516478.1:p.Ala404Val | |
| XM_011518178.2:c.860C>T | XP_011516480.1:p.Ala287Val | |
| XM_017014232.1:c.2183C>T | XP_016869721.1:p.Ala728Val | |
| XM_017014233.1:c.1805C>T | XP_016869722.1:p.Ala602Val | |
| XM_017014234.2:c.1205C>T | XP_016869723.1:p.Ala402Val | |
| XM_017014235.1:c.2195C>T | XP_016869724.1:p.Ala732Val | |
| XR_001746171.1:n.3194-2159C>T | ||
| NM_139026.5:c.2102C>T | NP_620595.1:p.Ala701Val | |
| NM_139027.5:c.2195C>T | NP_620596.2:p.Ala732Val | |
| NM_139025.5:c.2195C>T | NP_620594.1:p.Ala732Val | |
| NM_139026.6:c.2102C>T | NP_620595.1:p.Ala701Val | |
| NM_139027.6:c.2195C>T MANE Select | NP_620596.2:p.Ala732Val | |
| NR_024514.3:n.1258-2159C>T |