HGVS | Genome Assembly |
---|---|
NC_000009.12:g.134375567_134375575del , CM000671.2:g.134375567_134375575del | GRCh38 |
NC_000009.11:g.137267413_137267421del , CM000671.1:g.137267413_137267421del | GRCh37 |
NC_000009.10:g.136407234_136407242del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000481739.2:c.29-26065_29-26057del MANE Select | ENSP00000419692.1:n.29-26065_29-26057del | |
ENST00000356384.4:n.293+1437_293+1445del | ||
ENST00000481739.1:c.29-26065_29-26057del | ENSP00000419692.1:n.29-26065_29-26057del | |
ENST00000484822.1:n.453-26065_453-26057del | ||
NM_002957.5:c.29-26065_29-26057del | NP_002948.1:n.29-26065_29-26057del | |
NM_002957.6:c.29-26065_29-26057del MANE Select | NP_002948.1:n.29-26065_29-26057del |