HGVS | Genome Assembly |
---|---|
NC_000003.12:g.189995379T= , CM000665.2:g.189995379T= | GRCh38 |
NC_000003.11:g.189713168T= , CM000665.1:g.189713168T= | GRCh37 |
NC_000003.10:g.191195862T= | NCBI36 |
NG_031929.1:g.132059A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000319332.10:c.544A= MANE Select | ENSP00000316881.5:p.Met182= | |
ENST00000319332.9:c.544A= | ENSP00000316881.5:p.Met182= | |
ENST00000426003.1:c.1A= | ENSP00000394326.1:p.Met1= | |
ENST00000427335.6:c.1A= | ENSP00000408947.2:p.Met1= | |
ENST00000444866.5:c.1A= | ENSP00000391374.1:p.Met1= | |
NM_001134418.1:c.1A= | NP_001127890.1:p.Met1= | |
NM_018192.3:c.544A= | NP_060662.2:p.Met182= | |
XM_011512955.1:c.1A= | XP_011511257.1:p.Met1= | |
NM_018192.4:c.544A= MANE Select | NP_060662.2:p.Met182= | |
NM_001134418.2:c.1A= | NP_001127890.1:p.Met1= |