HGVS | Genome Assembly |
---|---|
NC_000009.12:g.12710090T= , CM000671.2:g.12710090T= | GRCh38 |
NC_000009.11:g.12710090T= , CM000671.1:g.12710090T= | GRCh37 |
NC_000009.10:g.12700090T= | NCBI36 |
NG_011705.1:g.21705T= |
HGVS | Amino-acid Change |
---|---|
NM_000550.3:c.*908T= (TYRP1) MANE Select | NP_000541.1:n.*908T= |
ENST00000388918.10:c.*908T= (TYRP1) MANE Select | ENSP00000373570.4:n.*908T= |
NM_000550.2:c.*908T= (TYRP1) | NP_000541.1:n.*908T= |
NR_125775.1:n.317-9464A= (LURAP1L-AS1) | |
ENST00000388918.9:c.*908T= (TYRP1) | ENSP00000373570.4:n.*908T= |