HGVS | Genome Assembly |
---|---|
NC_000019.10:g.10224503C>G , CM000681.2:g.10224503C>G | GRCh38 |
NC_000019.9:g.10335179C>G , CM000681.1:g.10335179C>G | GRCh37 |
NC_000019.8:g.10196179C>G | NCBI36 |
NG_028016.3:g.11784G>C , LRG_362:g.11784G>C | |
NG_046802.1:g.12305G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000646641.1:c.403G>C (S1PR2) MANE Select | ENSP00000496438.1:p.Ala135Pro | |
ENST00000588952.5:c.-401-5634G>C (DNMT1) | ENSP00000467050.1:n.-401-5634G>C | |
ENST00000590320.2:c.403G>C (S1PR2) | ENSP00000466933.1:p.Ala135Pro | |
ENST00000592342.5:c.-284+6701G>C (DNMT1) | ENSP00000465993.1:n.-284+6701G>C | |
NM_004230.3:c.403G>C (S1PR2) | NP_004221.3:p.Ala135Pro | |
XM_011528425.1:c.403G>C (S1PR2) | XP_011526727.1:p.Ala135Pro | |
NM_004230.4:c.403G>C (S1PR2) MANE Select | NP_004221.3:p.Ala135Pro |