Linked Data
ClinVar Variation Id:
2535719
ClinVar RCV Id:
RCV003261180
dbSNP Id:
rs763839239
ExAC:
17:7357742 T / C
gnomAD v2:
17-7357742-T-C
gnomAD v4:
17-7454423-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7454423T>C , CM000679.2:g.7454423T>C | GRCh38 |
| NC_000017.10:g.7357742T>C , CM000679.1:g.7357742T>C | GRCh37 |
| NC_000017.9:g.7298466T>C | NCBI36 |
| NG_008026.1:g.14337T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306071.7:c.947T>C MANE Select | ENSP00000304290.2:p.Met316Thr | |
| ENST00000306071.6:c.947T>C | ENSP00000304290.2:p.Met316Thr | |
| ENST00000536404.6:c.731T>C | ENSP00000439209.2:p.Met244Thr | |
| ENST00000570557.5:c.610T>C | ||
| ENST00000573209.1:n.1891T>C | ||
| ENST00000576360.1:c.605-21T>C | ENSP00000459092.1:n.605-21T>C | |
| NM_000747.2:c.947T>C | NP_000738.2:p.Met316Thr | |
| NM_000747.3:c.947T>C MANE Select | NP_000738.2:p.Met316Thr |