HGVS | Genome Assembly |
---|---|
NC_000003.12:g.143286378A= , CM000665.2:g.143286378A= | GRCh38 |
NC_000003.11:g.143005220A= , CM000665.1:g.143005220A= | GRCh37 |
NC_000003.10:g.144487910A= | NCBI36 |
NG_017077.1:g.567154T= | |
NG_017077.2:g.567154T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000316549.11:c.1605-17398T= MANE Select | ENSP00000320246.6:n.1605-17398T= | |
ENST00000316549.10:c.1605-17398T= | ENSP00000320246.6:n.1605-17398T= | |
NM_173653.3:c.1605-17398T= | NP_775924.1:n.1605-17398T= | |
XM_011512703.1:c.957-17398T= | XP_011511005.1:n.957-17398T= | |
XM_011512703.3:c.957-17398T= | XP_011511005.1:n.957-17398T= | |
XM_017006202.2:c.1712-2036T= | XP_016861691.1:n.1712-2036T= | |
XM_017006203.1:c.1254-17398T= | XP_016861692.1:n.1254-17398T= | |
NM_173653.4:c.1605-17398T= MANE Select | NP_775924.1:n.1605-17398T= |