HGVS | Genome Assembly |
---|---|
NC_000009.12:g.127854046dup , CM000671.2:g.127854046dup | GRCh38 |
NC_000009.11:g.130616325dup , CM000671.1:g.130616325dup | GRCh37 |
NC_000009.10:g.129656146dup | NCBI36 |
NG_009551.1:g.5723dup , LRG_589:g.5723dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373203.9:c.67+243dup MANE Select | ENSP00000362299.4:n.67+243dup | |
ENST00000344849.4:c.67+243dup | ENSP00000341917.3:n.67+243dup | |
ENST00000373203.8:c.67+243dup | ENSP00000362299.4:n.67+243dup | |
NM_000118.3:c.67+243dup , LRG_589t1:c.67+243dup | NP_000109.1:n.67+243dup | |
NM_001114753.2:c.67+243dup , LRG_589t2:c.67+243dup | NP_001108225.1:n.67+243dup | |
NM_001114753.3:c.67+243dup MANE Select | NP_001108225.1:n.67+243dup |