HGVS | Genome Assembly |
---|---|
NC_000018.10:g.13884578_13884579delinsCT , CM000680.2:g.13884578_13884579delinsCT | GRCh38 |
NC_000018.9:g.13884577_13884578delinsCT , CM000680.1:g.13884577_13884578delinsCT | GRCh37 |
NC_000018.8:g.13874577_13874578delinsCT | NCBI36 |
NG_011819.1:g.35958_35959delinsAG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000327606.4:c.*46_*47delinsAG MANE Select | ENSP00000333821.2:n.*46_*47delinsAG | |
ENST00000327606.3:c.*46_*47delinsAG | ENSP00000333821.2:n.*46_*47delinsAG | |
NM_000529.2:c.*46_*47delinsAG MANE Select | NP_000520.1:n.*46_*47delinsAG | |
NM_001291911.1:c.*46_*47delinsAG | NP_001278840.1:n.*46_*47delinsAG | |
XM_017025781.1:c.*46_*47delinsAG | XP_016881270.1:n.*46_*47delinsAG |