HGVS | Genome Assembly |
---|---|
NC_000018.10:g.24460649T= , CM000680.2:g.24460649T= | GRCh38 |
NC_000018.9:g.22040613T= , CM000680.1:g.22040613T= | GRCh37 |
NC_000018.8:g.20294611T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256906.5:c.-80T= MANE Select | ENSP00000256906.4:n.-80T= | |
ENST00000256906.4:c.-80T= | ENSP00000256906.4:n.-80T= | |
NM_001143828.1:c.-80T= | NP_001137300.1:n.-80T= | |
NM_001160166.1:c.-80T= | NP_001153638.1:n.-80T= | |
NM_021624.3:c.-80T= | NP_067637.2:n.-80T= | |
XM_011526133.1:c.-80T= | XP_011524435.1:n.-80T= | |
XM_011526134.1:c.-80T= | XP_011524436.1:n.-80T= | |
NM_021624.4:c.-80T= MANE Select | NP_067637.2:n.-80T= | |
NM_001143828.2:c.-80T= | NP_001137300.1:n.-80T= | |
NM_001160166.2:c.-80T= | NP_001153638.1:n.-80T= |