Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.119344744A>C , CM000673.2:g.119344744A>C | GRCh38 |
| NC_000011.9:g.119215454A>C , CM000673.1:g.119215454A>C | GRCh37 |
| NC_000011.8:g.118720664A>C | NCBI36 |
| NG_012235.1:g.6930T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000619721.6:c.786T>G (MFRP) MANE Select | ENSP00000481824.1:p.His262Gln | |
| ENST00000360167.4:c.786T>G (MFRP) | ENSP00000353291.4:p.His262Gln | |
| ENST00000529147.2:n.749T>G (MFRP) | ||
| ENST00000619721.5:c.786T>G (MFRP) | ENSP00000481824.1:p.His262Gln | |
| NM_015645.4:c.-1851T>G (C1QTNF5) | NP_056460.1:n.-1851T>G | |
| NM_031433.3:c.786T>G (MFRP) | NP_113621.1:p.His262Gln | |
| NM_031433.4:c.786T>G (MFRP) MANE Select | NP_113621.1:p.His262Gln | |
| NM_015645.5:c.-1851T>G (C1QTNF5) | NP_056460.1:n.-1851T>G |