HGVS | Genome Assembly |
---|---|
NC_000018.10:g.13884717_13884718delinsTG , CM000680.2:g.13884717_13884718delinsTG | GRCh38 |
NC_000018.9:g.13884716_13884717delinsTG , CM000680.1:g.13884716_13884717delinsTG | GRCh37 |
NC_000018.8:g.13874716_13874717delinsTG | NCBI36 |
NG_011819.1:g.35819_35820delinsCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327606.4:c.801_802delinsCA MANE Select | ENSP00000333821.2:p.Cys267= | |
ENST00000327606.3:c.801_802delinsCA | ENSP00000333821.2:p.Cys267= | |
NM_000529.2:c.801_802delinsCA MANE Select | NP_000520.1:p.Cys267= | |
NM_001291911.1:c.801_802delinsCA | NP_001278840.1:p.Cys267= | |
XM_017025781.1:c.801_802delinsCA | XP_016881270.1:p.Cys267= |