HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240873911del , CM000664.2:g.240873911del | GRCh38 |
NC_000002.11:g.241813328del , CM000664.1:g.241813328del | GRCh37 |
NC_000002.10:g.241462001del | NCBI36 |
NG_008005.1:g.10167del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000307503.4:c.596-67del MANE Select | ENSP00000302620.3:n.596-67del | |
ENST00000307503.3:c.596-67del | ENSP00000302620.3:n.596-67del | |
ENST00000476698.1:n.332+862del | ||
NM_000030.2:c.596-67del | NP_000021.1:n.596-67del | |
NM_000030.3:c.596-67del MANE Select | NP_000021.1:n.596-67del |