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:
102776
dbSNP Id:
rs62507319
gnomAD v4:
12-102855177-T-A
ERepo:
CA229681/MONDO:0009861/006
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102855177T>A , CM000674.2:g.102855177T>A | GRCh38 |
| NC_000012.11:g.103248955T>A , CM000674.1:g.103248955T>A | GRCh37 |
| NC_000012.10:g.101773085T>A | NCBI36 |
| NG_008690.1:g.67426A>T | |
| NG_008690.2:g.108234A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000553106.6:c.665A>T MANE Select | ENSP00000448059.1:p.Asp222Val | |
| ENST00000307000.7:c.650A>T | ENSP00000303500.2:p.Asp217Val | |
| ENST00000549111.5:n.761A>T | ||
| ENST00000553106.5:c.665A>T | ENSP00000448059.1:p.Asp222Val | |
| NM_000277.1:c.665A>T | NP_000268.1:p.Asp222Val | |
| XM_011538422.1:c.665A>T | XP_011536724.1:p.Asp222Val | |
| NM_000277.2:c.665A>T | NP_000268.1:p.Asp222Val | |
| NM_001354304.1:c.665A>T | NP_001341233.1:p.Asp222Val | |
| XM_017019370.2:c.665A>T | XP_016874859.1:p.Asp222Val | |
| NM_000277.3:c.665A>T MANE Select | NP_000268.1:p.Asp222Val | |
| NM_001354304.2:c.665A>T | NP_001341233.1:p.Asp222Val |