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:
1003866
ClinVar RCV Id:
RCV001300480
dbSNP Id:
rs774832953
ExAC:
1:115256439 G / A
gnomAD v2:
1-115256439-G-A
gnomAD v3:
1-114713818-G-A
gnomAD v4:
1-114713818-G-A
COSMIC:
COSM2177457
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114713818G>A , CM000663.2:g.114713818G>A | GRCh38 |
| NC_000001.10:g.115256439G>A , CM000663.1:g.115256439G>A | GRCh37 |
| NC_000001.9:g.115057962G>A | NCBI36 |
| NG_007572.1:g.8077C>T , LRG_92:g.8077C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000369535.5:c.272C>T MANE Select | ENSP00000358548.4:p.Ala91Val | |
| ENST00000369535.4:c.272C>T | ENSP00000358548.4:p.Ala91Val | |
| NM_002524.4:c.272C>T | NP_002515.1:p.Ala91Val | |
| NM_002524.5:c.272C>T MANE Select | NP_002515.1:p.Ala91Val |