HGVS | Genome Assembly |
---|---|
NC_000003.12:g.49828788_49828827del , CM000665.2:g.49828788_49828827del | GRCh38 |
NC_000003.11:g.49866221_49866260del , CM000665.1:g.49866221_49866260del | GRCh37 |
NC_000003.10:g.49841225_49841264del | NCBI36 |
NG_046695.1:g.32736_32775del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331456.7:c.*279_*318del MANE Select | ENSP00000328203.2:n.*279_*318del | |
ENST00000331456.6:c.*279_*318del | ENSP00000328203.2:n.*279_*318del | |
ENST00000491060.1:n.843_882del | ||
NM_005879.2:c.*279_*318del | NP_005870.2:n.*279_*318del | |
XM_011533264.1:c.*279_*318del | XP_011531566.1:n.*279_*318del | |
XM_017005526.1:c.*279_*318del | XP_016861015.1:n.*279_*318del | |
XR_001739979.1:n.1893_1932del | ||
NM_005879.3:c.*279_*318del MANE Select | NP_005870.2:n.*279_*318del |