HGVS | Genome Assembly |
---|---|
NC_000023.11:g.151177401C= , CM000685.2:g.151177401C= | GRCh38 |
NC_000023.10:g.150345873C= , CM000685.1:g.150345873C= | GRCh37 |
NC_000023.9:g.150096531C= | NCBI36 |
NG_016405.1:g.5818C= | |
NG_016405.2:g.5818C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000218316.4:c.187+493C= (GPR50) MANE Select | ENSP00000218316.3:n.187+493C= | |
ENST00000218316.3:c.187+493C= (GPR50) | ENSP00000218316.3:n.187+493C= | |
ENST00000617907.1:c.187+493C= (GPR50) | ENSP00000484496.1:n.187+493C= | |
NM_004224.3:c.187+493C= (GPR50) MANE Select | NP_004215.2:n.187+493C= | |
NR_135300.1:n.436G= (GPR50-AS1) |