HGVS | Genome Assembly |
---|---|
NC_000004.12:g.68560022C= , CM000666.2:g.68560022C= | GRCh38 |
NC_000004.11:g.69425740C= , CM000666.1:g.69425740C= | GRCh37 |
NC_000004.10:g.69108335C= | NCBI36 |
NG_017033.1:g.13506G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000317746.3:c.1005+515G= (UGT2B17) MANE Select | ENSP00000320401.2:n.1005+515G= | |
ENST00000684088.1:c.255+515G= (UGT2B17) | ENSP00000507374.1:n.255+515G= | |
ENST00000317746.2:c.1005+515G= (UGT2B17) | ENSP00000320401.2:n.1005+515G= | |
ENST00000616841.4:c.1733-22496G= (UGT2B15) | ENSP00000482004.1:n.1733-22496G= | |
NM_001077.3:c.1005+515G= (UGT2B17) | NP_001068.1:n.1005+515G= | |
XM_024454205.1:c.1005+515G= (UGT2B17) | XP_024309973.1:n.1005+515G= | |
NM_001077.4:c.1005+515G= (UGT2B17) MANE Select | NP_001068.1:n.1005+515G= |