Linked Data
gnomAD v4:
9-77794623-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.77794623C>T , CM000671.2:g.77794623C>T | GRCh38 |
| NC_000009.11:g.80409539C>T , CM000671.1:g.80409539C>T | GRCh37 |
| NC_000009.10:g.79599359C>T | NCBI36 |
| NG_027904.2:g.241681G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286548.9:c.606-31G>A MANE Select | ENSP00000286548.4:n.606-31G>A | |
| ENST00000286548.8:c.606-31G>A | ENSP00000286548.4:n.606-31G>A | |
| NM_002072.4:c.606-31G>A | NP_002063.2:n.606-31G>A | |
| XM_017014628.2:c.432-31G>A | XP_016870117.1:n.432-31G>A | |
| NM_002072.5:c.606-31G>A MANE Select | NP_002063.2:n.606-31G>A |