HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86739711del , CM000670.2:g.86739711del | GRCh38 |
NC_000008.10:g.87751939del , CM000670.1:g.87751939del | GRCh37 |
NC_000008.9:g.87821055del | NCBI36 |
NG_016980.1:g.8965del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000320005.6:c.155del MANE Select | ENSP00000316605.5:p.Ser52PhefsTer? | |
ENST00000681746.1:c.155del | ENSP00000505959.1:p.Ser52PhefsTer? | |
ENST00000320005.5:c.155del | ENSP00000316605.5:p.Ser52PhefsTer? | |
ENST00000519777.1:n.137del | ||
NM_019098.4:c.155del | NP_061971.3:p.Ser52PhefsTer? | |
NM_019098.5:c.155del MANE Select | NP_061971.3:p.Ser52PhefsTer? |