HGVS | Genome Assembly |
---|---|
NC_000009.12:g.91950010del , CM000671.2:g.91950010del | GRCh38 |
NC_000009.11:g.94712292del , CM000671.1:g.94712292del | GRCh37 |
NC_000009.10:g.93752113del | NCBI36 |
NG_008089.1:g.5156del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375708.4:c.-44del MANE Select | ENSP00000364860.3:n.-44del | |
ENST00000375708.3:c.-44del | ENSP00000364860.3:n.-44del | |
NM_004560.3:c.-44del | NP_004551.2:n.-44del | |
NM_001318204.1:c.-44del | NP_001305133.1:n.-44del | |
XR_001746315.1:n.200del | ||
NM_004560.4:c.-44del MANE Select | NP_004551.2:n.-44del | |
NM_001318204.2:c.-44del | NP_001305133.1:n.-44del |