HGVS | Genome Assembly |
---|---|
NC_000004.12:g.4862563_4862574del , CM000666.2:g.4862563_4862574del | GRCh38 |
NC_000004.11:g.4864290_4864301del , CM000666.1:g.4864290_4864301del | GRCh37 |
NC_000004.10:g.4915191_4915202del | NCBI36 |
NG_008121.1:g.7899_7910del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382723.5:c.470-138_470-127del MANE Select | ENSP00000372170.4:n.470-138_470-127del | |
ENST00000382723.4:c.470-138_470-127del | ENSP00000372170.4:n.470-138_470-127del | |
ENST00000468421.1:n.136_147del | ||
NM_002448.3:c.470-138_470-127del MANE Select | NP_002439.2:n.470-138_470-127del |