HGVS | Genome Assembly |
---|---|
NC_000009.12:g.12708102C>G , CM000671.2:g.12708102C>G | GRCh38 |
NC_000009.11:g.12708102C>G , CM000671.1:g.12708102C>G | GRCh37 |
NC_000009.10:g.12698102C>G | NCBI36 |
NG_011705.1:g.19717C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000388918.10:c.1367C>G (TYRP1) MANE Select | ENSP00000373570.4:p.Ala456Gly | |
ENST00000381136.2:c.497C>G (TYRP1) | ENSP00000370528.2:p.Ala166Gly | |
ENST00000381142.3:n.499-875C>G (TYRP1) | ||
ENST00000388918.9:c.1367C>G (TYRP1) | ENSP00000373570.4:p.Ala456Gly | |
ENST00000473504.1:n.432C>G (TYRP1) | ||
NM_000550.2:c.1367C>G (TYRP1) | NP_000541.1:p.Ala456Gly | |
NR_125775.1:n.317-7476G>C (LURAP1L-AS1) | ||
XR_001746372.2:n.1351C>G (TYRP1) | ||
NM_000550.3:c.1367C>G (TYRP1) MANE Select | NP_000541.1:p.Ala456Gly |