HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190426_204190427insCCCCCCCCCCCCCTC , CM000663.2:g.204190426_204190427insCCCCCCCCCCCCCTC | GRCh38 |
NC_000001.10:g.204159554_204159555insCCCCCCCCCCCCCTC , CM000663.1:g.204159554_204159555insCCCCCCCCCCCCCTC | GRCh37 |
NC_000001.9:g.202426177_202426178insCCCCCCCCCCCCCTC | NCBI36 |
NG_032151.1:g.11066_11067insAGGGGGGGGGGGGGG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367194.5:c.*58_*59insAGGGGGGGGGGGGGG MANE Select | ENSP00000356162.4:n.*58_*59insAGGGGGGGGGGGGGG | |
ENST00000367194.4:c.*58_*59insAGGGGGGGGGGGGGG | ENSP00000356162.4:n.*58_*59insAGGGGGGGGGGGGGG | |
NM_002256.3:c.*58_*59insAGGGGGGGGGGGGGG | NP_002247.3:n.*58_*59insAGGGGGGGGGGGGGG | |
XM_011509525.1:c.*58_*59insAGGGGGGGGGGGGGG | XP_011507827.1:n.*58_*59insAGGGGGGGGGGGGGG | |
NM_002256.4:c.*58_*59insAGGGGGGGGGGGGGG MANE Select | NP_002247.3:n.*58_*59insAGGGGGGGGGGGGGG |