Linked Data
ClinVar Variation Id:
13888
ClinVar RCV Id:
RCV000014902
dbSNP Id:
rs121913675
COSMIC:
COSM693
PubMed:
PMID:9927037
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.116778953C>T , CM000669.2:g.116778953C>T | GRCh38 |
| NC_000007.13:g.116419007C>T , CM000669.1:g.116419007C>T | GRCh37 |
| NC_000007.12:g.116206243C>T | NCBI36 |
| NG_008996.1:g.111549C>T , LRG_662:g.111549C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000436117.3:c.*1123C>T | ENSP00000410980.2:n.*1123C>T | |
| ENST00000318493.11:c.3572C>T | ENSP00000317272.6:p.Thr1191Ile | |
| ENST00000397752.8:c.3518C>T MANE Select | ENSP00000380860.3:p.Thr1173Ile | |
| ENST00000318493.10:c.3572C>T | ENSP00000317272.6:p.Thr1191Ile | |
| ENST00000397752.7:c.3518C>T | ENSP00000380860.3:p.Thr1173Ile | |
| NM_000245.2:c.3518C>T | NP_000236.2:p.Thr1173Ile | |
| NM_001127500.1:c.3572C>T , LRG_662t1:c.3572C>T | NP_001120972.1:p.Thr1191Ile | |
| XM_006715990.2:c.2228C>T | XP_006716053.1:p.Thr743Ile | |
| XM_006715991.2:c.2228C>T | XP_006716054.1:p.Thr743Ile | |
| XM_011516223.1:c.3575C>T | XP_011514525.1:p.Thr1192Ile | |
| NM_000245.3:c.3518C>T | NP_000236.2:p.Thr1173Ile | |
| NM_001127500.2:c.3572C>T | NP_001120972.1:p.Thr1191Ile | |
| NM_001324402.1:c.2228C>T | NP_001311331.1:p.Thr743Ile | |
| XR_001744772.1:n.3649C>T | ||
| NM_001127500.3:c.3572C>T | NP_001120972.1:p.Thr1191Ile | |
| NM_000245.4:c.3518C>T MANE Select | NP_000236.2:p.Thr1173Ile | |
| NM_001324402.2:c.2228C>T | NP_001311331.1:p.Thr743Ile |