Linked Data
gnomAD v4:
9-99221594-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.99221594C>T , CM000671.2:g.99221594C>T | GRCh38 |
| NC_000009.11:g.101983876C>T , CM000671.1:g.101983876C>T | GRCh37 |
| NC_000009.10:g.101023697C>T | NCBI36 |
| NG_008928.1:g.5371G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000476832.2:c.301G>A MANE Select | ENSP00000417764.1:p.Val101Met | |
| ENST00000238477.5:c.301G>A | ENSP00000432675.2:p.Val101Met | |
| ENST00000476832.1:c.301G>A | ENSP00000417764.1:p.Val101Met | |
| NM_033087.3:c.301G>A | NP_149078.1:p.Val101Met | |
| NR_024532.1:n.371G>A | ||
| NM_033087.4:c.301G>A MANE Select | NP_149078.1:p.Val101Met | |
| NR_024532.2:n.349G>A |