HGVS | Genome Assembly |
---|---|
NC_000023.11:g.116172604T= , CM000685.2:g.116172604T= | GRCh38 |
NC_000023.10:g.115303857T= , CM000685.1:g.115303857T= | GRCh37 |
NC_000023.9:g.115217885T= | NCBI36 |
NG_016326.1:g.6900T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371906.5:c.324T= MANE Select | ENSP00000360973.4:p.Tyr108= | |
ENST00000680409.1:n.792T= | ||
ENST00000681852.1:c.324T= | ENSP00000505750.1:p.Tyr108= | |
ENST00000371906.4:c.324T= | ENSP00000360973.4:p.Tyr108= | |
NM_000686.4:c.324T= | NP_000677.2:p.Tyr108= | |
XM_011537533.1:c.324T= | XP_011535835.1:p.Tyr108= | |
NM_000686.5:c.324T= MANE Select | NP_000677.2:p.Tyr108= | |
NM_001385624.1:c.324T= | NP_001372553.1:p.Tyr108= |