HGVS | Genome Assembly |
---|---|
NC_000001.11:g.152309003_152309014del , CM000663.2:g.152309003_152309014del | GRCh38 |
NC_000001.10:g.152281479_152281490del , CM000663.1:g.152281479_152281490del | GRCh37 |
NC_000001.9:g.150548103_150548114del | NCBI36 |
NG_016190.1:g.21191_21202del , LRG_1028:g.21191_21202del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368799.2:c.5873_5884del MANE Select | ENSP00000357789.1:p.Gly1958_His1961del | |
ENST00000368799.1:c.5873_5884del | ENSP00000357789.1:p.Gly1958_His1961del | |
NM_002016.1:c.5873_5884del , LRG_1028t1:c.5873_5884del | NP_002007.1:p.Gly1958_His1961del | |
XM_011509329.1:c.5873_5884del | XP_011507631.1:p.Gly1958_His1961del | |
NM_002016.2:c.5873_5884del MANE Select | NP_002007.1:p.Gly1958_His1961del |