HGVS | Genome Assembly |
---|---|
NC_000002.12:g.84425689_84425695dup , CM000664.2:g.84425689_84425695dup | GRCh38 |
NC_000002.11:g.84652813_84652819dup , CM000664.1:g.84652813_84652819dup | GRCh37 |
NC_000002.10:g.84506324_84506330dup | NCBI36 |
NG_016755.1:g.38778_38784dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000393868.7:c.826-82_826-76dup MANE Select | ENSP00000377446.2:n.826-82_826-76dup | |
ENST00000651342.1:c.*266-82_*266-76dup | ENSP00000498471.1:n.*266-82_*266-76dup | |
ENST00000393868.6:c.826-82_826-76dup | ENSP00000377446.2:n.826-82_826-76dup | |
ENST00000484365.1:n.1252_1258dup | ||
ENST00000487809.1:n.573-82_573-76dup | ||
ENST00000491123.5:n.672-82_672-76dup | ||
NM_003849.3:c.826-82_826-76dup | NP_003840.2:n.826-82_826-76dup | |
NM_003849.4:c.826-82_826-76dup MANE Select | NP_003840.2:n.826-82_826-76dup |