Linked Data
ClinVar Variation Id:
120277
ClinVar RCV Id:
RCV000106358
dbSNP Id:
rs281865455
ERepo:
CA267656/MONDO:0009861/006
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102866601G>T , CM000674.2:g.102866601G>T | GRCh38 |
| NC_000012.11:g.103260379G>T , CM000674.1:g.103260379G>T | GRCh37 |
| NC_000012.10:g.101784509G>T | NCBI36 |
| NG_008690.1:g.56002C>A | |
| NG_008690.2:g.96810C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.504C>A MANE Select | ENSP00000448059.1:p.Tyr168Ter | |
| ENST00000307000.7:c.489C>A | ENSP00000303500.2:p.Tyr163Ter | |
| ENST00000549111.5:n.600C>A | ||
| ENST00000551988.5:n.530+10861C>A | ||
| ENST00000553106.5:c.504C>A | ENSP00000448059.1:p.Tyr168Ter | |
| NM_000277.1:c.504C>A | NP_000268.1:p.Tyr168Ter | |
| XM_011538422.1:c.504C>A | XP_011536724.1:p.Tyr168Ter | |
| NM_000277.2:c.504C>A | NP_000268.1:p.Tyr168Ter | |
| NM_001354304.1:c.504C>A | NP_001341233.1:p.Tyr168Ter | |
| XM_017019370.2:c.504C>A | XP_016874859.1:p.Tyr168Ter | |
| NM_000277.3:c.504C>A MANE Select | NP_000268.1:p.Tyr168Ter | |
| NM_001354304.2:c.504C>A | NP_001341233.1:p.Tyr168Ter |