HGVS | Genome Assembly |
---|---|
NC_000013.11:g.33036547T= , CM000675.2:g.33036547T= | GRCh38 |
NC_000013.10:g.33610684T= , CM000675.1:g.33610684T= | GRCh37 |
NC_000013.9:g.32508684T= | NCBI36 |
NG_011485.1:g.25114T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000380099.4:c.820-17220T= MANE Select | ENSP00000369442.3:n.820-17220T= | |
ENST00000380099.3:c.820-17220T= | ENSP00000369442.3:n.820-17220T= | |
ENST00000487852.1:n.828-17220T= | ||
NM_004795.3:c.820-17220T= | NP_004786.2:n.820-17220T= | |
XM_006719895.1:c.-102-17220T= | XP_006719958.1:n.-102-17220T= | |
XM_006719895.2:c.-102-17220T= | XP_006719958.1:n.-102-17220T= | |
NM_004795.4:c.820-17220T= MANE Select | NP_004786.2:n.820-17220T= |