HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1444371_1444378del , CM000667.2:g.1444371_1444378del | GRCh38 |
NC_000005.9:g.1444486_1444493del , CM000667.1:g.1444486_1444493del | GRCh37 |
NC_000005.8:g.1497486_1497493del | NCBI36 |
NG_015885.1:g.6052_6059del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270349.12:c.-46+971_-46+978del MANE Select | ENSP00000270349.9:n.-46+971_-46+978del | |
ENST00000270349.11:c.-46+971_-46+978del | ENSP00000270349.9:n.-46+971_-46+978del | |
NM_001044.4:c.-46+971_-46+978del | NP_001035.1:n.-46+971_-46+978del | |
NM_001044.5:c.-46+971_-46+978del MANE Select | NP_001035.1:n.-46+971_-46+978del |