Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.26912036C= , CM000663.2:g.26912036C= | GRCh38 |
| NC_000001.10:g.27238527C= , CM000663.1:g.27238527C= | GRCh37 |
| NC_000001.9:g.27111114C= | NCBI36 |
| NG_012143.1:g.7041G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_021969.3:c.583G= (NR0B2) MANE Select | NP_068804.1:p.Ala195= |
| ENST00000254227.4:c.583G= (NR0B2) MANE Select | ENSP00000254227.3:p.Ala195= |
| NM_021969.2:c.583G= (NR0B2) | NP_068804.1:p.Ala195= |
| ENST00000254227.3:c.583G= (NR0B2) | ENSP00000254227.3:p.Ala195= |
| ENST00000435827.6:c.93+801C= (NUDC) | ENSP00000404020.2:n.93+801C= |
| XM_011540529.1:c.93+801C= (NUDC) | XP_011538831.1:n.93+801C= |
| XM_017000094.1:c.93+801C= (NUDC) | XP_016855583.1:n.93+801C= |
| XM_024452486.1:c.93+801C= (NUDC) | XP_024308254.1:n.93+801C= |