HGVS | Genome Assembly |
---|---|
NC_000009.12:g.12708121C>T , CM000671.2:g.12708121C>T | GRCh38 |
NC_000009.11:g.12708121C>T , CM000671.1:g.12708121C>T | GRCh37 |
NC_000009.10:g.12698121C>T | NCBI36 |
NG_011705.1:g.19736C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000388918.10:c.1386C>T (TYRP1) MANE Select | ENSP00000373570.4:p.Tyr462= | |
ENST00000381136.2:c.516C>T (TYRP1) | ENSP00000370528.2:p.Tyr172= | |
ENST00000381142.3:n.499-856C>T (TYRP1) | ||
ENST00000388918.9:c.1386C>T (TYRP1) | ENSP00000373570.4:p.Tyr462= | |
ENST00000473504.1:n.451C>T (TYRP1) | ||
NM_000550.2:c.1386C>T (TYRP1) | NP_000541.1:p.Tyr462= | |
NR_125775.1:n.317-7495G>A (LURAP1L-AS1) | ||
XR_001746372.2:n.1370C>T (TYRP1) | ||
NM_000550.3:c.1386C>T (TYRP1) MANE Select | NP_000541.1:p.Tyr462= |