Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.151880628T>C , CM000665.2:g.151880628T>C | GRCh38 |
| NC_000003.11:g.151598416T>C , CM000665.1:g.151598416T>C | GRCh37 |
| NC_000003.10:g.153081106T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000362032.6:c.85T>C (SUCNR1) MANE Select | ENSP00000355156.4:p.Phe29Leu | |
| NM_033050.4:c.85T>C (SUCNR1) | NP_149039.2:p.Phe29Leu | |
| NR_110202.1:n.319+47229A>G (AADACL2-AS1) | ||
| NR_110203.1:n.319+47229A>G (AADACL2-AS1) | ||
| NM_033050.5:c.85T>C (SUCNR1) | NP_149039.2:p.Phe29Leu | |
| NM_033050.6:c.85T>C (SUCNR1) MANE Select | NP_149039.2:p.Phe29Leu |