Linked Data
gnomAD v4:
9-77794678-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.77794678G>T , CM000671.2:g.77794678G>T | GRCh38 |
| NC_000009.11:g.80409594G>T , CM000671.1:g.80409594G>T | GRCh37 |
| NC_000009.10:g.79599414G>T | NCBI36 |
| NG_027904.2:g.241626C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286548.9:c.606-86C>A MANE Select | ENSP00000286548.4:n.606-86C>A | |
| ENST00000286548.8:c.606-86C>A | ENSP00000286548.4:n.606-86C>A | |
| NM_002072.4:c.606-86C>A | NP_002063.2:n.606-86C>A | |
| XM_017014628.2:c.432-86C>A | XP_016870117.1:n.432-86C>A | |
| NM_002072.5:c.606-86C>A MANE Select | NP_002063.2:n.606-86C>A |