HGVS | Genome Assembly |
---|---|
NC_000010.11:g.93601656A>C , CM000672.2:g.93601656A>C | GRCh38 |
NC_000010.10:g.95361413A>C , CM000672.1:g.95361413A>C | GRCh37 |
NC_000010.9:g.95351403A>C | NCBI36 |
NG_009104.1:g.4581T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371467.5:c.-313T>G (RBP4) | ENSP00000360522.1:n.-313T>G | |
ENST00000371469.2:c.51+10T>G (RBP4) | ENSP00000360524.2:n.51+10T>G | |
ENST00000604414.1:c.697-2418A>C (FFAR4) | ENSP00000474477.1:n.697-2418A>C | |
ENST00000629763.2:c.47+14T>G (RBP4) | ENSP00000487033.1:n.47+14T>G | |
NM_001323518.1:c.51+10T>G (RBP4) | NP_001310447.1:n.51+10T>G | |
NM_001323518.2:c.51+10T>G (RBP4) | NP_001310447.1:n.51+10T>G |