HGVS | Genome Assembly |
---|---|
NC_000008.11:g.42839199T= , CM000670.2:g.42839199T= | GRCh38 |
NC_000008.10:g.42694342T= , CM000670.1:g.42694342T= | GRCh37 |
NC_000008.9:g.42813499T= | NCBI36 |
NG_011837.1:g.9133A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254250.7:c.254A= MANE Select | ENSP00000254250.3:p.Glu85= | |
ENST00000345117.2:c.72-863A= | ENSP00000344966.2:n.72-863A= | |
ENST00000529779.1:c.254A= | ENSP00000433912.1:p.Glu85= | |
NM_018105.2:c.254A= | NP_060575.1:p.Glu85= | |
NM_199003.1:c.72-863A= | NP_945354.1:n.72-863A= | |
NM_018105.3:c.254A= MANE Select | NP_060575.1:p.Glu85= | |
NM_199003.2:c.72-863A= | NP_945354.1:n.72-863A= |