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:
2848615
ClinVar RCV Id:
RCV003695324
dbSNP Id:
rs1483062041
gnomAD v2:
2-26703741-G-A
gnomAD v4:
2-26480873-G-A
COSMIC:
COSM5058841
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.26480873G>A , CM000664.2:g.26480873G>A | GRCh38 |
| NC_000002.11:g.26703741G>A , CM000664.1:g.26703741G>A | GRCh37 |
| NC_000002.10:g.26557245G>A | NCBI36 |
| NG_009937.1:g.82826C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000272371.7:c.1716C>T MANE Select | ENSP00000272371.2:p.Gly572= | |
| ENST00000272371.6:c.1716C>T | ENSP00000272371.2:p.Gly572= | |
| ENST00000403946.7:c.1716C>T | ENSP00000385255.3:p.Gly572= | |
| NM_001287489.1:c.1716C>T | NP_001274418.1:p.Gly572= | |
| NM_194248.2:c.1716C>T | NP_919224.1:p.Gly572= | |
| XM_005264644.2:c.1761C>T | XP_005264701.1:p.Gly587= | |
| XM_011533185.1:c.1761C>T | XP_011531487.1:p.Gly587= | |
| XM_017005338.1:c.1716C>T | XP_016860827.1:p.Gly572= | |
| NM_001287489.2:c.1716C>T | NP_001274418.1:p.Gly572= | |
| NM_194248.3:c.1716C>T MANE Select | NP_919224.1:p.Gly572= |