HGVS | Genome Assembly |
---|---|
NC_000013.11:g.27924464_27924466del , CM000675.2:g.27924464_27924466del | GRCh38 |
NC_000013.10:g.28498601_28498603del , CM000675.1:g.28498601_28498603del | GRCh37 |
NC_000013.9:g.27396601_27396603del | NCBI36 |
NG_008183.1:g.9434_9436del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381033.5:c.615_617del MANE Select | ENSP00000370421.4:p.Glu205del | |
ENST00000381033.4:c.615_617del | ENSP00000370421.4:p.Glu205del | |
NM_000209.3:c.615_617del | NP_000200.1:p.Glu205del | |
NM_000209.4:c.615_617del MANE Select | NP_000200.1:p.Glu205del |