Linked Data
gnomAD v4:
9-133644290-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133644290G>A , CM000671.2:g.133644290G>A | GRCh38 |
| NC_000009.11:g.136509412G>A , CM000671.1:g.136509412G>A | GRCh37 |
| NC_000009.10:g.135499233G>A | NCBI36 |
| NG_008645.1:g.12928G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000393056.8:c.994G>A MANE Select | ENSP00000376776.2:p.Val332Ile | |
| ENST00000393056.6:c.994G>A | ENSP00000376776.2:p.Val332Ile | |
| NM_000787.3:c.994G>A | NP_000778.3:p.Val332Ile | |
| NM_000787.4:c.994G>A MANE Select | NP_000778.3:p.Val332Ile |