HGVS | Genome Assembly |
---|---|
NC_000002.12:g.84425675_84425676del , CM000664.2:g.84425675_84425676del | GRCh38 |
NC_000002.11:g.84652799_84652800del , CM000664.1:g.84652799_84652800del | GRCh37 |
NC_000002.10:g.84506310_84506311del | NCBI36 |
NG_016755.1:g.38789_38790del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000393868.7:c.826-71_826-70del MANE Select | ENSP00000377446.2:n.826-71_826-70del | |
ENST00000651342.1:c.*266-71_*266-70del | ENSP00000498471.1:n.*266-71_*266-70del | |
ENST00000393868.6:c.826-71_826-70del | ENSP00000377446.2:n.826-71_826-70del | |
ENST00000484365.1:n.1263_1264del | ||
ENST00000487809.1:n.573-71_573-70del | ||
ENST00000491123.5:n.672-71_672-70del | ||
NM_003849.3:c.826-71_826-70del | NP_003840.2:n.826-71_826-70del | |
NM_003849.4:c.826-71_826-70del MANE Select | NP_003840.2:n.826-71_826-70del |