HGVS | Genome Assembly |
---|---|
NC_000009.12:g.12707990A>C , CM000671.2:g.12707990A>C | GRCh38 |
NC_000009.11:g.12707990A>C , CM000671.1:g.12707990A>C | GRCh37 |
NC_000009.10:g.12697990A>C | NCBI36 |
NG_011705.1:g.19605A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000388918.10:c.1262-7A>C (TYRP1) MANE Select | ENSP00000373570.4:n.1262-7A>C | |
ENST00000381136.2:c.392-7A>C (TYRP1) | ENSP00000370528.2:n.392-7A>C | |
ENST00000381142.3:n.499-987A>C (TYRP1) | ||
ENST00000388918.9:c.1262-7A>C (TYRP1) | ENSP00000373570.4:n.1262-7A>C | |
ENST00000473504.1:n.320A>C (TYRP1) | ||
NM_000550.2:c.1262-7A>C (TYRP1) | NP_000541.1:n.1262-7A>C | |
NR_125775.1:n.317-7364T>G (LURAP1L-AS1) | ||
XR_001746372.2:n.1246-7A>C (TYRP1) | ||
NM_000550.3:c.1262-7A>C (TYRP1) MANE Select | NP_000541.1:n.1262-7A>C |