HGVS | Genome Assembly |
---|---|
NC_000009.12:g.12704549T>A , CM000671.2:g.12704549T>A | GRCh38 |
NC_000009.11:g.12704549T>A , CM000671.1:g.12704549T>A | GRCh37 |
NC_000009.10:g.12694549T>A | NCBI36 |
NG_011705.1:g.16164T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000388918.10:c.1105T>A (TYRP1) MANE Select | ENSP00000373570.4:p.Tyr369Asn | |
ENST00000381136.2:c.235T>A (TYRP1) | ENSP00000370528.2:p.Tyr79Asn | |
ENST00000381142.3:n.342T>A (TYRP1) | ||
ENST00000388918.9:c.1105T>A (TYRP1) | ENSP00000373570.4:p.Tyr369Asn | |
NM_000550.2:c.1105T>A (TYRP1) | NP_000541.1:p.Tyr369Asn | |
NR_125775.1:n.317-3923A>T (LURAP1L-AS1) | ||
XR_001746372.2:n.1089T>A (TYRP1) | ||
NM_000550.3:c.1105T>A (TYRP1) MANE Select | NP_000541.1:p.Tyr369Asn |