HGVS | Genome Assembly |
---|---|
NC_000017.11:g.16948776T= , CM000679.2:g.16948776T= | GRCh38 |
NC_000017.10:g.16852090T= , CM000679.1:g.16852090T= | GRCh37 |
NC_000017.9:g.16792815T= | NCBI36 |
NG_007281.1:g.28313A= , LRG_120:g.28313A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261652.7:c.407A= MANE Select | ENSP00000261652.2:p.Tyr136= | |
ENST00000261652.6:c.407A= | ENSP00000261652.2:p.Tyr136= | |
ENST00000579315.5:c.407A= | ENSP00000464069.1:p.Tyr136= | |
ENST00000581616.2:n.410A= | ||
ENST00000582931.5:n.311A= | ||
ENST00000583789.1:c.269A= | ENSP00000462952.1:p.Tyr90= | |
ENST00000584950.5:c.269A= | ENSP00000463582.1:p.Tyr90= | |
NM_012452.2:c.407A= , LRG_120t1:c.407A= | NP_036584.1:p.Tyr136= | |
NM_012452.3:c.407A= MANE Select | NP_036584.1:p.Tyr136= |