HGVS | Genome Assembly |
---|---|
NC_000023.11:g.116173583_116173584insAG , CM000685.2:g.116173583_116173584insAG | GRCh38 |
NC_000023.10:g.115304836_115304837insAG , CM000685.1:g.115304836_115304837insAG | GRCh37 |
NC_000023.9:g.115218864_115218865insAG | NCBI36 |
NG_016326.1:g.7879_7880insAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371906.5:c.*211_*212insAG MANE Select | ENSP00000360973.4:n.*211_*212insAG | |
ENST00000371906.4:c.*211_*212insAG | ENSP00000360973.4:n.*211_*212insAG | |
NM_000686.4:c.*211_*212insAG | NP_000677.2:n.*211_*212insAG | |
XM_011537533.1:c.*211_*212insAG | XP_011535835.1:n.*211_*212insAG | |
NM_000686.5:c.*211_*212insAG MANE Select | NP_000677.2:n.*211_*212insAG | |
NM_001385624.1:c.*211_*212insAG | NP_001372553.1:n.*211_*212insAG |