HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190426_204190427insCCCCCCCCCCCCCCCTCC , CM000663.2:g.204190426_204190427insCCCCCCCCCCCCCCCTCC | GRCh38 |
NC_000001.10:g.204159554_204159555insCCCCCCCCCCCCCCCTCC , CM000663.1:g.204159554_204159555insCCCCCCCCCCCCCCCTCC | GRCh37 |
NC_000001.9:g.202426177_202426178insCCCCCCCCCCCCCCCTCC | NCBI36 |
NG_032151.1:g.11067_11068insAGGGGGGGGGGGGGGGGG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367194.5:c.*59_*60insAGGGGGGGGGGGGGGGGG MANE Select | ENSP00000356162.4:n.*59_*60insAGGGGGGGGGGGGGGGGG | |
ENST00000367194.4:c.*59_*60insAGGGGGGGGGGGGGGGGG | ENSP00000356162.4:n.*59_*60insAGGGGGGGGGGGGGGGGG | |
NM_002256.3:c.*59_*60insAGGGGGGGGGGGGGGGGG | NP_002247.3:n.*59_*60insAGGGGGGGGGGGGGGGGG | |
XM_011509525.1:c.*59_*60insAGGGGGGGGGGGGGGGGG | XP_011507827.1:n.*59_*60insAGGGGGGGGGGGGGGGGG | |
NM_002256.4:c.*59_*60insAGGGGGGGGGGGGGGGGG MANE Select | NP_002247.3:n.*59_*60insAGGGGGGGGGGGGGGGGG |