HGVS | Genome Assembly |
---|---|
NC_000007.14:g.77133485_77133488dup , CM000669.2:g.77133485_77133488dup | GRCh38 |
NC_000007.13:g.76762802_76762805dup , CM000669.1:g.76762802_76762805dup | GRCh37 |
NC_000007.12:g.76600738_76600741dup | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000285871.5:c.-12+10753_-12+10756dup MANE Select | ENSP00000285871.4:n.-12+10753_-12+10756dup | |
ENST00000285871.4:c.-12+10753_-12+10756dup | ENSP00000285871.4:n.-12+10753_-12+10756dup | |
ENST00000415750.5:c.-12+11017_-12+11020dup | ENSP00000388649.1:n.-12+11017_-12+11020dup | |
NM_020879.2:c.-12+10753_-12+10756dup | NP_065930.2:n.-12+10753_-12+10756dup | |
XR_927691.1:n.48-4762_48-4759dup | ||
NM_020879.3:c.-12+10753_-12+10756dup MANE Select | NP_065930.2:n.-12+10753_-12+10756dup |