Linked Data
gnomAD v4:
9-99221627-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.99221627C>T , CM000671.2:g.99221627C>T | GRCh38 |
| NC_000009.11:g.101983909C>T , CM000671.1:g.101983909C>T | GRCh37 |
| NC_000009.10:g.101023730C>T | NCBI36 |
| NG_008928.1:g.5338G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000476832.2:c.268G>A MANE Select | ENSP00000417764.1:p.Ala90Thr | |
| ENST00000238477.5:c.268G>A | ENSP00000432675.2:p.Ala90Thr | |
| ENST00000476832.1:c.268G>A | ENSP00000417764.1:p.Ala90Thr | |
| NM_033087.3:c.268G>A | NP_149078.1:p.Ala90Thr | |
| NR_024532.1:n.338G>A | ||
| NM_033087.4:c.268G>A MANE Select | NP_149078.1:p.Ala90Thr | |
| NR_024532.2:n.316G>A |