HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128357395T= , CM000667.2:g.128357395T= | GRCh38 |
NC_000005.9:g.127693087T= , CM000667.1:g.127693087T= | GRCh37 |
NC_000005.8:g.127720986T= | NCBI36 |
NG_008750.1:g.185649A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262464.9:c.2555A= MANE Select | ENSP00000262464.4:p.Asp852= | |
ENST00000262464.8:c.2555A= | ENSP00000262464.4:p.Asp852= | |
ENST00000508053.5:c.2555A= | ENSP00000424571.1:p.Asp852= | |
ENST00000508989.5:c.2456A= | ENSP00000425596.1:p.Asp819= | |
ENST00000619499.4:c.2552A= | ENSP00000482132.1:p.Asp851= | |
NM_001999.3:c.2555A= | NP_001990.2:p.Asp852= | |
XM_017009228.2:c.2402A= | XP_016864717.1:p.Asp801= | |
NM_001999.4:c.2555A= MANE Select | NP_001990.2:p.Asp852= |