HGVS | Genome Assembly |
---|---|
NC_000001.11:g.186673794T= , CM000663.2:g.186673794T= | GRCh38 |
NC_000001.10:g.186642926T= , CM000663.1:g.186642926T= | GRCh37 |
NC_000001.9:g.184909549T= | NCBI36 |
NG_028206.2:g.11634A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367468.10:c.*559A= MANE Select | ENSP00000356438.5:n.*559A= | |
ENST00000680451.1:c.*559A= | ENSP00000506242.1:n.*559A= | |
ENST00000681605.1:c.*2046A= | ENSP00000504900.1:n.*2046A= | |
ENST00000367468.9:c.*559A= | ENSP00000356438.5:n.*559A= | |
ENST00000490885.6:n.2789A= | ||
NM_000963.3:c.*559A= | NP_000954.1:n.*559A= | |
NM_000963.4:c.*559A= MANE Select | NP_000954.1:n.*559A= |