Linked Data
ClinVar Variation Id:
189474
ClinVar RCV Id:
RCV000169864
RCV000491290
RCV000499784
RCV000552740
RCV002505225
RCV003231353
RCV003462271
RCV003313047
dbSNP Id:
rs398123317
gnomAD v4:
10-87925550-T-C
COSMIC:
COSM5036
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87925550T>C , CM000672.2:g.87925550T>C | GRCh38 |
| NC_000010.10:g.89685307T>C , CM000672.1:g.89685307T>C | GRCh37 |
| NC_000010.9:g.89675287T>C | NCBI36 |
| NG_007466.2:g.67112T>C , LRG_311:g.67112T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700029.2:c.202T>C | ENSP00000514759.2:p.Tyr68His | |
| ENST00000710265.1:c.202T>C | ENSP00000518161.1:p.Tyr68His | |
| ENST00000472832.3:c.202T>C | ENSP00000483066.2:p.Tyr68His | |
| ENST00000688158.2:n.937T>C | ||
| ENST00000688922.2:c.202T>C | ENSP00000508742.2:p.Tyr68His | |
| ENST00000700021.1:c.165-5496T>C | ENSP00000514757.1:n.165-5496T>C | |
| ENST00000700022.1:c.202T>C | ENSP00000514758.1:p.Tyr68His | |
| ENST00000700029.1:c.36T>C | ||
| ENST00000706954.1:c.202T>C | ENSP00000516674.1:p.Tyr68His | |
| ENST00000706955.1:c.*237T>C | ENSP00000516675.1:n.*237T>C | |
| ENST00000686459.1:c.202T>C | ENSP00000508909.1:p.Tyr68His | |
| ENST00000688158.1:c.*313T>C | ENSP00000509254.1:n.*313T>C | |
| ENST00000688308.1:c.202T>C | ENSP00000508752.1:p.Tyr68His | |
| ENST00000688922.1:c.71T>C | ||
| ENST00000693560.1:c.721T>C | ENSP00000509861.1:p.Tyr241His | |
| ENST00000371953.8:c.202T>C MANE Select | ENSP00000361021.3:p.Tyr68His | |
| ENST00000371953.7:c.202T>C | ENSP00000361021.3:p.Tyr68His | |
| ENST00000498703.1:n.28T>C | ||
| ENST00000610634.1:c.100T>C | ENSP00000477517.1:p.Tyr34His | |
| NM_000314.5:c.202T>C | NP_000305.3:p.Tyr68His | |
| NM_000314.6:c.202T>C | NP_000305.3:p.Tyr68His | |
| NM_001304717.2:c.721T>C | NP_001291646.2:p.Tyr241His | |
| NM_001304718.1:c.-541-5496T>C | NP_001291647.1:n.-541-5496T>C | |
| XM_006717926.2:c.165-5496T>C | XP_006717989.1:n.165-5496T>C | |
| XM_011539981.1:c.202T>C | XP_011538283.1:p.Tyr68His | |
| XM_011539982.1:c.106T>C | XP_011538284.1:p.Tyr36His | |
| XR_945789.1:n.914T>C | ||
| XR_945790.1:n.914T>C | ||
| XR_945791.1:n.914T>C | ||
| NM_000314.7:c.202T>C | NP_000305.3:p.Tyr68His | |
| NM_001304717.5:c.721T>C | NP_001291646.4:p.Tyr241His | |
| NM_001304718.2:c.-541-5496T>C | NP_001291647.1:n.-541-5496T>C | |
| NM_000314.8:c.202T>C MANE Select | NP_000305.3:p.Tyr68His |