HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99949772_99949774del , CM000666.2:g.99949772_99949774del | GRCh38 |
NC_000004.11:g.100870929_100870931del , CM000666.1:g.100870929_100870931del | GRCh37 |
NC_000004.10:g.101089952_101089954del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296417.6:c.4-28_4-26del MANE Select | ENSP00000296417.5:n.4-28_4-26del | |
ENST00000651623.1:c.4-28_4-26del | ENSP00000498935.1:n.4-28_4-26del | |
ENST00000296417.5:c.4-28_4-26del | ENSP00000296417.5:n.4-28_4-26del | |
ENST00000511203.1:n.532_534del | ||
ENST00000511319.5:n.501_503del | ||
ENST00000511348.1:n.189-28_189-26del | ||
ENST00000527366.1:n.88-28_88-26del | ||
ENST00000529158.5:n.53-28_53-26del | ||
NM_002106.3:c.4-28_4-26del | NP_002097.1:n.4-28_4-26del | |
NM_002106.4:c.4-28_4-26del MANE Select | NP_002097.1:n.4-28_4-26del |