HGVS | Genome Assembly |
---|---|
NC_000017.11:g.29530377T= , CM000679.2:g.29530377T= | GRCh38 |
NC_000017.10:g.27857395T= , CM000679.1:g.27857395T= | GRCh37 |
NC_000017.9:g.24881521T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261716.8:c.2149-30T= MANE Select | ENSP00000261716.3:n.2149-30T= | |
ENST00000261716.7:c.2149-30T= | ENSP00000261716.3:n.2149-30T= | |
ENST00000536202.1:c.1705-30T= | ENSP00000438819.1:n.1705-30T= | |
ENST00000578653.1:n.233-30T= | ||
NM_020791.2:c.2149-30T= | NP_065842.1:n.2149-30T= | |
NM_025142.1:c.1705-30T= | NP_079418.1:n.1705-30T= | |
XM_011525060.1:c.2149-30T= | XP_011523362.1:n.2149-30T= | |
XM_011525060.2:c.2149-30T= | XP_011523362.1:n.2149-30T= | |
NM_020791.4:c.2149-30T= MANE Select | NP_065842.1:n.2149-30T= |