HGVS | Genome Assembly |
---|---|
NC_000022.11:g.27750779_27750781dup , CM000684.2:g.27750779_27750781dup | GRCh38 |
NC_000022.10:g.28146767_28146769dup , CM000684.1:g.28146767_28146769dup | GRCh37 |
NC_000022.9:g.26476767_26476769dup | NCBI36 |
NG_023258.1:g.55718_55720dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000703102.1:n.622_624dup | ||
ENST00000302326.5:c.*134_*136dup MANE Select | ENSP00000304956.4:n.*134_*136dup | |
ENST00000302326.4:c.*134_*136dup | ENSP00000304956.4:n.*134_*136dup | |
ENST00000424656.1:c.450_452dup | ||
ENST00000497225.1:n.453_455dup | ||
NM_002430.2:c.*134_*136dup | NP_002421.3:n.*134_*136dup | |
NM_002430.3:c.*134_*136dup MANE Select | NP_002421.3:n.*134_*136dup |