HGVS | Genome Assembly |
---|---|
NC_000023.11:g.116172592T= , CM000685.2:g.116172592T= | GRCh38 |
NC_000023.10:g.115303845T= , CM000685.1:g.115303845T= | GRCh37 |
NC_000023.9:g.115217873T= | NCBI36 |
NG_016326.1:g.6888T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371906.5:c.312T= MANE Select | ENSP00000360973.4:p.Tyr104= | |
ENST00000680409.1:n.780T= | ||
ENST00000681852.1:c.312T= | ENSP00000505750.1:p.Tyr104= | |
ENST00000371906.4:c.312T= | ENSP00000360973.4:p.Tyr104= | |
NM_000686.4:c.312T= | NP_000677.2:p.Tyr104= | |
XM_011537533.1:c.312T= | XP_011535835.1:p.Tyr104= | |
NM_000686.5:c.312T= MANE Select | NP_000677.2:p.Tyr104= | |
NM_001385624.1:c.312T= | NP_001372553.1:p.Tyr104= |