HGVS | Genome Assembly |
---|---|
NC_000004.12:g.68567480A= , CM000666.2:g.68567480A= | GRCh38 |
NC_000004.11:g.69433198A= , CM000666.1:g.69433198A= | GRCh37 |
NC_000004.10:g.69115793A= | NCBI36 |
NG_017033.1:g.6048T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000317746.3:c.724+281T= (UGT2B17) MANE Select | ENSP00000320401.2:n.724+281T= | |
ENST00000684088.1:c.-26-1760T= (UGT2B17) | ENSP00000507374.1:n.-26-1760T= | |
ENST00000317746.2:c.724+281T= (UGT2B17) | ENSP00000320401.2:n.724+281T= | |
ENST00000616841.4:c.1733-29954T= (UGT2B15) | ENSP00000482004.1:n.1733-29954T= | |
NM_001077.3:c.724+281T= (UGT2B17) | NP_001068.1:n.724+281T= | |
XM_024454205.1:c.724+281T= (UGT2B17) | XP_024309973.1:n.724+281T= | |
NM_001077.4:c.724+281T= (UGT2B17) MANE Select | NP_001068.1:n.724+281T= |