HGVS | Genome Assembly |
---|---|
NC_000020.11:g.33443656_33443657del , CM000682.2:g.33443656_33443657del | GRCh38 |
NC_000020.10:g.32031462_32031463del , CM000682.1:g.32031462_32031463del | GRCh37 |
NC_000020.9:g.31495123_31495124del | NCBI36 |
NG_011622.1:g.5236_5237del , LRG_332:g.5236_5237del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000217381.3:c.-37_-36del MANE Select | ENSP00000217381.2:n.-37_-36del | |
ENST00000217381.2:c.-37_-36del | ENSP00000217381.2:n.-37_-36del | |
NM_003098.2:c.-37_-36del , LRG_332t1:c.-37_-36del | NP_003089.1:n.-37_-36del | |
XM_005260517.1:c.-37_-36del | XP_005260574.1:n.-37_-36del | |
XM_011529007.1:c.-37_-36del | XP_011527309.1:n.-37_-36del | |
XM_011529008.1:c.-37_-36del | XP_011527310.1:n.-37_-36del | |
XR_936612.1:n.197_198del | ||
NM_003098.3:c.-37_-36del MANE Select | NP_003089.1:n.-37_-36del |