Linked Data
ClinVar Variation Id:
8713
ClinVar RCV Id:
RCV000009251
dbSNP Id:
rs104893868
PubMed:
PMID:7581449
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52028799A>C , CM000666.2:g.52028799A>C | GRCh38 |
| NC_000004.11:g.52894965A>C , CM000666.1:g.52894965A>C | GRCh37 |
| NC_000004.10:g.52589722A>C | NCBI36 |
| NG_008891.1:g.14521T>G , LRG_204:g.14521T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000381431.10:c.552T>G MANE Select | ENSP00000370839.6:p.Tyr184Ter | |
| ENST00000381431.9:c.552T>G | ENSP00000370839.5:p.Tyr184Ter | |
| ENST00000506357.5:c.635T>G | ||
| NM_000232.4:c.552T>G , LRG_204t1:c.552T>G | NP_000223.1:p.Tyr184Ter | |
| XM_006714049.2:c.255T>G | XP_006714112.1:p.Tyr85Ter | |
| XM_011534403.1:c.342T>G | XP_011532705.1:p.Tyr114Ter | |
| XM_011534404.1:c.255T>G | XP_011532706.1:p.Tyr85Ter | |
| NM_000232.5:c.552T>G MANE Select | NP_000223.1:p.Tyr184Ter |