Linked Data
ClinVar Variation Id:
2916432
ClinVar RCV Id:
RCV003627524
dbSNP Id:
rs915983905
gnomAD v3:
18-31592977-C-T
gnomAD v4:
18-31592977-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31592977C>T , CM000680.2:g.31592977C>T | GRCh38 |
| NC_000018.9:g.29172940C>T , CM000680.1:g.29172940C>T | GRCh37 |
| NC_000018.8:g.27426938C>T | NCBI36 |
| NG_009490.1:g.6211C>T , LRG_416:g.6211C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000237014.8:c.151C>T MANE Select | ENSP00000237014.4:p.His51Tyr | |
| ENST00000610404.5:c.55C>T | ENSP00000477599.2:p.His19Tyr | |
| ENST00000649620.1:c.151C>T | ENSP00000497927.1:p.His51Tyr | |
| ENST00000237014.7:c.151C>T | ENSP00000237014.3:p.His51Tyr | |
| ENST00000432547.7:n.177C>T | ||
| ENST00000541025.2:n.177C>T | ||
| ENST00000610404.4:c.151C>T | ENSP00000477599.1:p.His51Tyr | |
| ENST00000613781.1:c.151C>T | ENSP00000479174.1:p.His51Tyr | |
| NM_000371.3:c.151C>T , LRG_416t1:c.151C>T | NP_000362.1:p.His51Tyr | |
| NM_000371.4:c.151C>T MANE Select | NP_000362.1:p.His51Tyr |