HGVS | Genome Assembly |
---|---|
NC_000014.9:g.21312487T= , CM000676.2:g.21312487T= | GRCh38 |
NC_000014.8:g.21780646T= , CM000676.1:g.21780646T= | GRCh37 |
NC_000014.7:g.20850486T= | NCBI36 |
NG_008933.1:g.29511T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000400017.7:c.1132T= MANE Select | ENSP00000382895.2:p.Tyr378= | |
ENST00000400017.6:c.1132T= | ENSP00000382895.2:p.Tyr378= | |
ENST00000556336.5:c.1051T= | ENSP00000450445.1:p.Tyr351= | |
ENST00000557771.5:c.1051T= | ENSP00000451219.1:p.Tyr351= | |
NM_020366.3:c.1132T= | NP_065099.3:p.Tyr378= | |
XM_011536983.1:c.1099T= | XP_011535285.1:p.Tyr367= | |
NM_020366.4:c.1132T= MANE Select | NP_065099.3:p.Tyr378= |