Linked Data
ClinVar Variation Id:
858685
dbSNP Id:
rs776362922
ExAC:
7:128477745 C / T
gnomAD v2:
7-128477745-C-T
gnomAD v3:
7-128837691-C-T
gnomAD v4:
7-128837691-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128837691C>T , CM000669.2:g.128837691C>T | GRCh38 |
| NC_000007.13:g.128477745C>T , CM000669.1:g.128477745C>T | GRCh37 |
| NC_000007.12:g.128264981C>T | NCBI36 |
| NG_011807.1:g.12263C>T , LRG_870:g.12263C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325888.13:c.905C>T MANE Select | ENSP00000327145.8:p.Thr302Met | |
| ENST00000325888.12:c.905C>T | ENSP00000327145.8:p.Thr302Met | |
| ENST00000346177.6:c.905C>T | ENSP00000344002.6:p.Thr302Met | |
| NM_001127487.1:c.905C>T | NP_001120959.1:p.Thr302Met | |
| NM_001458.4:c.905C>T , LRG_870t1:c.905C>T | NP_001449.3:p.Thr302Met | |
| NM_001127487.2:c.905C>T | NP_001120959.1:p.Thr302Met | |
| NM_001458.5:c.905C>T MANE Select | NP_001449.3:p.Thr302Met |