HGVS | Genome Assembly |
---|---|
NC_000010.11:g.93601654C>T , CM000672.2:g.93601654C>T | GRCh38 |
NC_000010.10:g.95361411C>T , CM000672.1:g.95361411C>T | GRCh37 |
NC_000010.9:g.95351401C>T | NCBI36 |
NG_009104.1:g.4583G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371467.5:c.-311G>A (RBP4) | ENSP00000360522.1:n.-311G>A | |
ENST00000371469.2:c.51+12G>A (RBP4) | ENSP00000360524.2:n.51+12G>A | |
ENST00000604414.1:c.697-2420C>T (FFAR4) | ENSP00000474477.1:n.697-2420C>T | |
ENST00000629763.2:c.47+16G>A (RBP4) | ENSP00000487033.1:n.47+16G>A | |
NM_001323518.1:c.51+12G>A (RBP4) | NP_001310447.1:n.51+12G>A | |
NM_001323518.2:c.51+12G>A (RBP4) | NP_001310447.1:n.51+12G>A |