HGVS | Genome Assembly |
---|---|
NC_000010.11:g.133532181A= , CM000672.2:g.133532181A= | GRCh38 |
NC_000010.10:g.135345685A= , CM000672.1:g.135345685A= | GRCh37 |
NC_000010.9:g.135195675A= | NCBI36 |
NG_008383.1:g.9819A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000252945.8:c.545A= MANE Select | ENSP00000252945.3:p.Asp182= | |
ENST00000252945.7:c.545A= | ENSP00000252945.3:p.Asp182= | |
ENST00000368520.1:n.606A= | ||
ENST00000418356.1:c.134A= | ENSP00000397299.1:p.Asp45= | |
ENST00000421586.5:c.284A= | ENSP00000412754.1:p.Asp95= | |
ENST00000463117.6:c.545A= | ENSP00000440689.1:p.Asp182= | |
ENST00000477500.5:n.448+447A= | ||
ENST00000541080.5:c.226+447A= | ||
NM_000773.3:c.545A= | NP_000764.1:p.Asp182= | |
NM_000773.4:c.545A= MANE Select | NP_000764.1:p.Asp182= |