HGVS | Genome Assembly |
---|---|
NC_000009.12:g.12708089A>G , CM000671.2:g.12708089A>G | GRCh38 |
NC_000009.11:g.12708089A>G , CM000671.1:g.12708089A>G | GRCh37 |
NC_000009.10:g.12698089A>G | NCBI36 |
NG_011705.1:g.19704A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000388918.10:c.1354A>G (TYRP1) MANE Select | ENSP00000373570.4:p.Met452Val | |
ENST00000381136.2:c.484A>G (TYRP1) | ENSP00000370528.2:p.Met162Val | |
ENST00000381142.3:n.499-888A>G (TYRP1) | ||
ENST00000388918.9:c.1354A>G (TYRP1) | ENSP00000373570.4:p.Met452Val | |
ENST00000473504.1:n.419A>G (TYRP1) | ||
NM_000550.2:c.1354A>G (TYRP1) | NP_000541.1:p.Met452Val | |
NR_125775.1:n.317-7463T>C (LURAP1L-AS1) | ||
XR_001746372.2:n.1338A>G (TYRP1) | ||
NM_000550.3:c.1354A>G (TYRP1) MANE Select | NP_000541.1:p.Met452Val |