Linked Data
gnomAD v4:
10-94781857-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94781857C>A , CM000672.2:g.94781857C>A | GRCh38 |
| NC_000010.10:g.96541614C>A , CM000672.1:g.96541614C>A | GRCh37 |
| NC_000010.9:g.96531604C>A | NCBI36 |
| NG_008384.2:g.24152C>A | |
| NG_008384.3:g.24177C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.679C>A MANE Select | ENSP00000360372.3:p.Pro227Thr | |
| ENST00000645461.1:n.1732C>A | ||
| ENST00000371321.7:c.679C>A | ENSP00000360372.3:p.Pro227Thr | |
| ENST00000464755.1:c.1442C>A | ENSP00000483243.1:n.1442C>A | |
| NM_000769.2:c.679C>A | NP_000760.1:p.Pro227Thr | |
| NM_000769.4:c.679C>A MANE Select | NP_000760.1:p.Pro227Thr |