HGVS | Genome Assembly |
---|---|
NC_000002.12:g.43887014_43887015dup , CM000664.2:g.43887014_43887015dup | GRCh38 |
NC_000002.11:g.44114153_44114154dup , CM000664.1:g.44114153_44114154dup | GRCh37 |
NC_000002.10:g.43967657_43967658dup | NCBI36 |
NG_008247.1:g.113992_113993dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682612.1:c.2538_2539dup | ||
ENST00000684454.1:n.9635_9636dup | ||
ENST00000260665.12:c.*1586_*1587dup MANE Select | ENSP00000260665.7:n.*1586_*1587dup | |
ENST00000260665.11:c.*1586_*1587dup | ENSP00000260665.7:n.*1586_*1587dup | |
NM_133259.3:c.*1586_*1587dup | NP_573566.2:n.*1586_*1587dup | |
XR_002958896.1:n.5953_5954dup | ||
NM_133259.4:c.*1586_*1587dup MANE Select | NP_573566.2:n.*1586_*1587dup |