Linked Data
ClinVar Variation Id:
767434
dbSNP Id:
rs200832069
ExAC:
9:101304179 C / T
gnomAD v2:
9-101304179-C-T
gnomAD v3:
9-98541897-C-T
gnomAD v4:
9-98541897-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.98541897C>T , CM000671.2:g.98541897C>T | GRCh38 |
| NC_000009.11:g.101304179C>T , CM000671.1:g.101304179C>T | GRCh37 |
| NC_000009.10:g.100344000C>T | NCBI36 |
| NG_016426.1:g.172301G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259455.4:c.606G>A MANE Select | ENSP00000259455.2:p.Thr202= | |
| ENST00000637410.1:n.384G>A | ||
| ENST00000637717.1:c.222G>A | ENSP00000490789.1:p.Thr74= | |
| ENST00000259455.3:c.606G>A | ENSP00000259455.2:p.Thr202= | |
| ENST00000477471.1:n.393G>A | ||
| ENST00000634227.1:n.380G>A | ||
| NM_005458.7:c.606G>A | NP_005449.5:p.Thr202= | |
| XM_017015331.2:c.312G>A | XP_016870820.1:p.Thr104= | |
| NM_005458.8:c.606G>A MANE Select | NP_005449.5:p.Thr202= |