HGVS | Genome Assembly |
---|---|
NC_000013.11:g.20188390T= , CM000675.2:g.20188390T= | GRCh38 |
NC_000013.10:g.20762529T= , CM000675.1:g.20762529T= | GRCh37 |
NC_000013.9:g.19660529T= | NCBI36 |
NG_008358.1:g.9586A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000382844.2:c.*511A= | ENSP00000372295.1:n.*511A= | |
ENST00000382848.5:c.*511A= MANE Select | ENSP00000372299.4:n.*511A= | |
ENST00000382844.1:c.*511A= | ENSP00000372295.1:n.*511A= | |
ENST00000382848.4:c.*511A= | ENSP00000372299.4:n.*511A= | |
NM_004004.5:c.*511A= | NP_003995.2:n.*511A= | |
XM_011535049.1:c.*511A= | XP_011533351.1:n.*511A= | |
XM_011535049.2:c.*511A= | XP_011533351.1:n.*511A= | |
NM_004004.6:c.*511A= MANE Select | NP_003995.2:n.*511A= |