Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.68567374C= , CM000666.2:g.68567374C= | GRCh38 |
| NC_000004.11:g.69433092C= , CM000666.1:g.69433092C= | GRCh37 |
| NC_000004.10:g.69115687C= | NCBI36 |
| NG_017033.1:g.6154G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000317746.3:c.724+387G= (UGT2B17) MANE Select | ENSP00000320401.2:n.724+387G= | |
| ENST00000684088.1:c.-26-1654G= (UGT2B17) | ENSP00000507374.1:n.-26-1654G= | |
| ENST00000317746.2:c.724+387G= (UGT2B17) | ENSP00000320401.2:n.724+387G= | |
| ENST00000616841.4:c.1733-29848G= (UGT2B15) | ENSP00000482004.1:n.1733-29848G= | |
| NM_001077.3:c.724+387G= (UGT2B17) | NP_001068.1:n.724+387G= | |
| XM_024454205.1:c.724+387G= (UGT2B17) | XP_024309973.1:n.724+387G= | |
| NM_001077.4:c.724+387G= (UGT2B17) MANE Select | NP_001068.1:n.724+387G= |