HGVS | Genome Assembly |
---|---|
NC_000023.11:g.116173577_116173578del , CM000685.2:g.116173577_116173578del | GRCh38 |
NC_000023.10:g.115304830_115304831del , CM000685.1:g.115304830_115304831del | GRCh37 |
NC_000023.9:g.115218858_115218859del | NCBI36 |
NG_016326.1:g.7873_7874del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371906.5:c.*205_*206del MANE Select | ENSP00000360973.4:n.*205_*206del | |
ENST00000371906.4:c.*205_*206del | ENSP00000360973.4:n.*205_*206del | |
NM_000686.4:c.*205_*206del | NP_000677.2:n.*205_*206del | |
XM_011537533.1:c.*205_*206del | XP_011535835.1:n.*205_*206del | |
NM_000686.5:c.*205_*206del MANE Select | NP_000677.2:n.*205_*206del | |
NM_001385624.1:c.*205_*206del | NP_001372553.1:n.*205_*206del |