HGVS | Genome Assembly |
---|---|
NC_000002.12:g.26135193_26135195del , CM000664.2:g.26135193_26135195del | GRCh38 |
NC_000002.11:g.26358062_26358064del , CM000664.1:g.26358062_26358064del | GRCh37 |
NC_000002.10:g.26211566_26211568del | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264710.5:c.*172_*174del MANE Select | ENSP00000264710.4:n.*172_*174del | |
ENST00000264710.4:c.*172_*174del | ENSP00000264710.4:n.*172_*174del | |
ENST00000495146.5:n.1138_1140del | ||
NM_016131.4:c.*172_*174del | NP_057215.3:n.*172_*174del | |
XM_024452565.1:c.*172_*174del | XP_024308333.1:n.*172_*174del | |
NM_016131.5:c.*172_*174del MANE Select | NP_057215.3:n.*172_*174del |