HGVS | Genome Assembly |
---|---|
NC_000001.11:g.152311048_152311049delinsAG , CM000663.2:g.152311048_152311049delinsAG | GRCh38 |
NC_000001.10:g.152283524_152283525delinsAG , CM000663.1:g.152283524_152283525delinsAG | GRCh37 |
NC_000001.9:g.150550148_150550149delinsAG | NCBI36 |
NG_016190.1:g.19155_19156delinsCT , LRG_1028:g.19155_19156delinsCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368799.2:c.3837_3838delinsCT MANE Select | ENSP00000357789.1:p.His1279= | |
ENST00000368799.1:c.3837_3838delinsCT | ENSP00000357789.1:p.His1279= | |
NM_002016.1:c.3837_3838delinsCT , LRG_1028t1:c.3837_3838delinsCT | NP_002007.1:p.His1279= | |
XM_011509329.1:c.3837_3838delinsCT | XP_011507631.1:p.His1279= | |
NM_002016.2:c.3837_3838delinsCT MANE Select | NP_002007.1:p.His1279= |