HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91107217_91107224dup , CM000674.2:g.91107217_91107224dup | GRCh38 |
NC_000012.11:g.91500994_91501001dup , CM000674.1:g.91500994_91501001dup | GRCh37 |
NC_000012.10:g.90025125_90025132dup | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000266718.5:c.862+901_862+908dup MANE Select | ENSP00000266718.4:n.862+901_862+908dup | |
ENST00000266718.4:c.862+901_862+908dup | ENSP00000266718.4:n.862+901_862+908dup | |
ENST00000546642.1:n.612+901_612+908dup | ||
ENST00000548071.1:n.255+901_255+908dup | ||
NM_002345.3:c.862+901_862+908dup | NP_002336.1:n.862+901_862+908dup | |
NM_002345.4:c.862+901_862+908dup MANE Select | NP_002336.1:n.862+901_862+908dup |