HGVS | Genome Assembly |
---|---|
NC_000024.10:g.6872490G= , CM000686.2:g.6872490G= | GRCh38 |
NC_000024.9:g.6740531G= , CM000686.1:g.6740531G= | GRCh37 |
NC_000024.8:g.6800531G= | NCBI36 |
NG_008011.1:g.6538C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000651267.2:c.54+65C= MANE Select | ENSP00000498344.1:n.54+65C= | |
ENST00000215479.10:c.54+65C= | ENSP00000215479.5:n.54+65C= | |
ENST00000651267.1:c.54+65C= | ENSP00000498344.1:n.54+65C= | |
ENST00000215479.9:c.54+65C= | ENSP00000215479.5:n.54+65C= | |
ENST00000383036.1:c.54+65C= | ENSP00000372505.1:n.54+65C= | |
NM_001143.1:c.54+65C= | NP_001134.1:n.54+65C= | |
XM_011531472.1:c.54+65C= | XP_011529774.1:n.54+65C= | |
NM_001364814.1:c.54+65C= | NP_001351743.1:n.54+65C= | |
NM_001143.2:c.54+65C= MANE Select | NP_001134.1:n.54+65C= |