Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.68539752T>C , CM000666.2:g.68539752T>C | GRCh38 |
| NC_000004.11:g.69405470T>C , CM000666.1:g.69405470T>C | GRCh37 |
| NC_000004.10:g.69088065T>C | NCBI36 |
| NG_017033.1:g.33776A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001077.4:c.1314-1848A>G (UGT2B17) MANE Select | NP_001068.1:n.1314-1848A>G |
| ENST00000317746.3:c.1314-1848A>G (UGT2B17) MANE Select | ENSP00000320401.2:n.1314-1848A>G |
| NM_001077.3:c.1314-1848A>G (UGT2B17) | NP_001068.1:n.1314-1848A>G |
| ENST00000317746.2:c.1314-1848A>G (UGT2B17) | ENSP00000320401.2:n.1314-1848A>G |
| ENST00000616841.4:c.1733-2226A>G (UGT2B15) | ENSP00000482004.1:n.1733-2226A>G |
| XM_024454205.1:c.1314-1848A>G (UGT2B17) | XP_024309973.1:n.1314-1848A>G |