HGVS | Genome Assembly |
---|---|
NC_000023.11:g.116173450_116173451insCC , CM000685.2:g.116173450_116173451insCC | GRCh38 |
NC_000023.10:g.115304703_115304704insCC , CM000685.1:g.115304703_115304704insCC | GRCh37 |
NC_000023.9:g.115218731_115218732insCC | NCBI36 |
NG_016326.1:g.7746_7747insCC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371906.5:c.*78_*79insCC MANE Select | ENSP00000360973.4:n.*78_*79insCC | |
ENST00000371906.4:c.*78_*79insCC | ENSP00000360973.4:n.*78_*79insCC | |
NM_000686.4:c.*78_*79insCC | NP_000677.2:n.*78_*79insCC | |
XM_011537533.1:c.*78_*79insCC | XP_011535835.1:n.*78_*79insCC | |
NM_000686.5:c.*78_*79insCC MANE Select | NP_000677.2:n.*78_*79insCC | |
NM_001385624.1:c.*78_*79insCC | NP_001372553.1:n.*78_*79insCC |