HGVS | Genome Assembly |
---|---|
NC_000002.12:g.176093623A= , CM000664.2:g.176093623A= | GRCh38 |
NC_000002.11:g.176958351A= , CM000664.1:g.176958351A= | GRCh37 |
NC_000002.10:g.176666597A= | NCBI36 |
NG_008137.1:g.5820A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000392539.4:c.733A= MANE Select | ENSP00000376322.3:p.Thr245= | |
ENST00000392539.3:c.733A= | ENSP00000376322.3:p.Thr245= | |
NM_000523.3:c.733A= | NP_000514.2:p.Thr245= | |
XM_011511068.1:c.725-857A= | XP_011509370.1:n.725-857A= | |
XM_011511068.2:c.725-857A= | XP_011509370.1:n.725-857A= | |
NM_000523.4:c.733A= MANE Select | NP_000514.2:p.Thr245= |