HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73322622_73322624del , CM000677.2:g.73322622_73322624del | GRCh38 |
NC_000015.9:g.73614963_73614965del , CM000677.1:g.73614963_73614965del | GRCh37 |
NC_000015.8:g.71402016_71402018del | NCBI36 |
NG_009063.1:g.51643_51645del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.3471_3473del MANE Select | ENSP00000261917.3:p.Ser1158del | |
ENST00000261917.3:c.3471_3473del | ENSP00000261917.3:p.Ser1158del | |
NM_005477.2:c.3471_3473del | NP_005468.1:p.Ser1158del | |
XM_011521148.1:c.2253_2255del | XP_011519450.1:p.Ser752del | |
XM_011521148.2:c.2253_2255del | XP_011519450.1:p.Ser752del | |
NM_005477.3:c.3471_3473del MANE Select | NP_005468.1:p.Ser1158del |