HGVS | Genome Assembly |
---|---|
NC_000023.11:g.139537151T= , CM000685.2:g.139537151T= | GRCh38 |
NC_000023.10:g.138619310T= , CM000685.1:g.138619310T= | GRCh37 |
NC_000023.9:g.138446976T= | NCBI36 |
NG_007994.1:g.11416T= , LRG_556:g.11416T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000218099.7:c.230T= MANE Select | ENSP00000218099.2:p.Val77= | |
ENST00000218099.6:c.230T= | ENSP00000218099.2:p.Val77= | |
ENST00000394090.2:c.230T= | ENSP00000377650.2:p.Val77= | |
ENST00000479617.2:n.237T= | ||
NM_000133.3:c.230T= , LRG_556t1:c.230T= | NP_000124.1:p.Val77= | |
NM_001313913.1:c.230T= | NP_001300842.1:p.Val77= | |
XM_005262397.3:c.230T= | XP_005262454.1:p.Val77= | |
XM_005262397.4:c.230T= | XP_005262454.1:p.Val77= | |
NM_000133.4:c.230T= MANE Select | NP_000124.1:p.Val77= | |
NM_001313913.2:c.230T= | NP_001300842.1:p.Val77= |