HGVS | Genome Assembly |
---|---|
NC_000023.11:g.116173599_116173600del , CM000685.2:g.116173599_116173600del | GRCh38 |
NC_000023.10:g.115304852_115304853del , CM000685.1:g.115304852_115304853del | GRCh37 |
NC_000023.9:g.115218880_115218881del | NCBI36 |
NG_016326.1:g.7895_7896del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371906.5:c.*227_*228del MANE Select | ENSP00000360973.4:n.*227_*228del | |
ENST00000371906.4:c.*227_*228del | ENSP00000360973.4:n.*227_*228del | |
NM_000686.4:c.*227_*228del | NP_000677.2:n.*227_*228del | |
XM_011537533.1:c.*227_*228del | XP_011535835.1:n.*227_*228del | |
NM_000686.5:c.*227_*228del MANE Select | NP_000677.2:n.*227_*228del | |
NM_001385624.1:c.*227_*228del | NP_001372553.1:n.*227_*228del |