HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122461760del , CM000672.2:g.122461760del | GRCh38 |
NC_000010.10:g.124221276del , CM000672.1:g.124221276del | GRCh37 |
NC_000010.9:g.124211266del | NCBI36 |
NG_011554.1:g.5236del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000368984.8:c.108del MANE Select | ENSP00000357980.3:p.Cys37AlafsTer? | |
ENST00000648167.1:c.154+3051del | ENSP00000498033.1:n.154+3051del | |
ENST00000368984.7:c.108del | ENSP00000357980.3:p.Cys37AlafsTer? | |
NM_002775.4:c.108del | NP_002766.1:p.Cys37AlafsTer? | |
NM_002775.5:c.108del MANE Select | NP_002766.1:p.Cys37AlafsTer? |