HGVS | Genome Assembly |
---|---|
NC_000004.12:g.68569184G>A , CM000666.2:g.68569184G>A | GRCh38 |
NC_000004.11:g.69434902G>A , CM000666.1:g.69434902G>A | GRCh37 |
NC_000004.10:g.69117497G>A | NCBI36 |
NG_017033.1:g.4344C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000317746.3:c.-64-636C>T (UGT2B17) MANE Select | ENSP00000320401.2:n.-64-636C>T | |
ENST00000684088.1:c.-26-3464C>T (UGT2B17) | ENSP00000507374.1:n.-26-3464C>T | |
ENST00000616841.4:c.1733-31658C>T (UGT2B15) | ENSP00000482004.1:n.1733-31658C>T | |
XM_024454205.1:c.-64-636C>T (UGT2B17) | XP_024309973.1:n.-64-636C>T | |
NM_001077.4:c.-64-636C>T (UGT2B17) MANE Select | NP_001068.1:n.-64-636C>T |