HGVS | Genome Assembly |
---|---|
NC_000018.10:g.13885124_13885125delinsAT , CM000680.2:g.13885124_13885125delinsAT | GRCh38 |
NC_000018.9:g.13885123_13885124delinsAT , CM000680.1:g.13885123_13885124delinsAT | GRCh37 |
NC_000018.8:g.13875123_13875124delinsAT | NCBI36 |
NG_011819.1:g.35412_35413delinsAT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327606.4:c.394_395delinsAT MANE Select | ENSP00000333821.2:p.Ile132= | |
ENST00000327606.3:c.394_395delinsAT | ENSP00000333821.2:p.Ile132= | |
NM_000529.2:c.394_395delinsAT MANE Select | NP_000520.1:p.Ile132= | |
NM_001291911.1:c.394_395delinsAT | NP_001278840.1:p.Ile132= | |
XM_017025781.1:c.394_395delinsAT | XP_016881270.1:p.Ile132= |