Linked Data
gnomAD v4:
9-129818860-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.129818860A>C , CM000671.2:g.129818860A>C | GRCh38 |
| NC_000009.11:g.132581139A>C , CM000671.1:g.132581139A>C | GRCh37 |
| NC_000009.10:g.131620960A>C | NCBI36 |
| NG_008049.1:g.10303T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000351698.5:c.505T>G MANE Select | ENSP00000345719.4:p.Phe169Val | |
| ENST00000651202.1:c.601T>G | ENSP00000498222.1:p.Phe201Val | |
| ENST00000351698.4:c.505T>G | ENSP00000345719.4:p.Phe169Val | |
| ENST00000473604.2:n.615T>G | ||
| NM_000113.2:c.505T>G | NP_000104.1:p.Phe169Val | |
| XR_929731.1:n.665T>G | ||
| XR_929731.3:n.533T>G | ||
| NM_000113.3:c.505T>G MANE Select | NP_000104.1:p.Phe169Val |