HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149884757_149884758delinsAG , CM000663.2:g.149884757_149884758delinsAG | GRCh38 |
NC_000001.10:g.149856307_149856308delinsAG , CM000663.1:g.149856307_149856308delinsAG | GRCh37 |
NC_000001.9:g.148122931_148122932delinsAG | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369155.4:c.*1502_*1503delinsCT MANE Select | ENSP00000358151.2:n.*1502_*1503delinsCT | |
ENST00000369155.3:c.*1502_*1503delinsCT | ENSP00000358151.2:n.*1502_*1503delinsCT | |
ENST00000369160.3:c.377+1506_377+1507delinsCT | ENSP00000375736.2:n.377+1506_377+1507deli... | |
NM_003528.2:c.*1502_*1503delinsCT | NP_003519.1:n.*1502_*1503delinsCT | |
NM_003528.3:c.*1502_*1503delinsCT MANE Select | NP_003519.1:n.*1502_*1503delinsCT |