Linked Data
ClinVar Variation Id:
133082
dbSNP Id:
rs193922883
PubMed:
PMID:15731587
ERepo:
CA024202/MONDO:0018493/012
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38580497T>C , CM000681.2:g.38580497T>C | GRCh38 |
| NC_000019.9:g.39071137T>C , CM000681.1:g.39071137T>C | GRCh37 |
| NC_000019.8:g.43762977T>C | NCBI36 |
| NG_008866.1:g.151798T>C , LRG_766:g.151798T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000593677.2:c.1575T>C | ||
| ENST00000688602.1:c.2972T>C | ||
| ENST00000689936.1:c.2944T>C | ||
| ENST00000359596.8:c.14639T>C MANE Select | ENSP00000352608.2:p.Met4880Thr | |
| ENST00000355481.8:c.14624T>C | ENSP00000347667.3:p.Met4875Thr | |
| ENST00000359596.7:c.14639T>C | ENSP00000352608.2:p.Met4880Thr | |
| ENST00000360985.7:c.14621T>C | ENSP00000354254.4:p.Met4874Thr | |
| NM_000540.2:c.14639T>C , LRG_766t1:c.14639T>C | NP_000531.2:p.Met4880Thr | |
| NM_001042723.1:c.14624T>C | NP_001036188.1:p.Met4875Thr | |
| XM_006723317.1:c.14621T>C | XP_006723380.1:p.Met4874Thr | |
| XM_006723319.1:c.14606T>C | XP_006723382.1:p.Met4869Thr | |
| XM_011527204.1:c.14636T>C | XP_011525506.1:p.Met4879Thr | |
| XM_011527205.1:c.14552T>C | XP_011525507.1:p.Met4851Thr | |
| XM_006723317.2:c.14621T>C | XP_006723380.1:p.Met4874Thr | |
| XM_006723319.2:c.14606T>C | XP_006723382.1:p.Met4869Thr | |
| XM_011527205.2:c.14552T>C | XP_011525507.1:p.Met4851Thr | |
| NM_000540.3:c.14639T>C MANE Select | NP_000531.2:p.Met4880Thr | |
| NM_001042723.2:c.14624T>C | NP_001036188.1:p.Met4875Thr |