Linked Data
ClinVar Variation Id:
904356
ClinVar RCV Id:
RCV001152222
dbSNP Id:
rs1190889679
gnomAD v2:
5-145719498-C-T
COSMIC:
COSM1696474
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.146339935C>T , CM000667.2:g.146339935C>T | GRCh38 |
| NC_000005.9:g.145719498C>T , CM000667.1:g.145719498C>T | GRCh37 |
| NC_000005.8:g.145699691C>T | NCBI36 |
| NG_011885.1:g.5912C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000646991.2:c.508C>T MANE Select | ENSP00000495718.1:p.His170Tyr | |
| ENST00000230732.4:c.508C>T | ENSP00000230732.4:p.His170Tyr | |
| NM_002700.2:c.508C>T | NP_002691.1:p.His170Tyr | |
| NM_002700.3:c.508C>T MANE Select | NP_002691.1:p.His170Tyr |