Linked Data
dbSNP Id:
rs770993888
ExAC:
10:96541703 C / T
gnomAD v2:
10-96541703-C-T
gnomAD v4:
10-94781946-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94781946C>T , CM000672.2:g.94781946C>T | GRCh38 |
| NC_000010.10:g.96541703C>T , CM000672.1:g.96541703C>T | GRCh37 |
| NC_000010.9:g.96531693C>T | NCBI36 |
| NG_008384.2:g.24241C>T | |
| NG_008384.3:g.24266C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.768C>T MANE Select | ENSP00000360372.3:p.Asp256= | |
| ENST00000645461.1:n.1821C>T | ||
| ENST00000371321.7:c.768C>T | ENSP00000360372.3:p.Asp256= | |
| ENST00000464755.1:c.1531C>T | ENSP00000483243.1:n.1531C>T | |
| NM_000769.2:c.768C>T | NP_000760.1:p.Asp256= | |
| NM_000769.4:c.768C>T MANE Select | NP_000760.1:p.Asp256= |