HGVS | Genome Assembly |
---|---|
NC_000010.11:g.93601658A= , CM000672.2:g.93601658A= | GRCh38 |
NC_000010.10:g.95361415A= , CM000672.1:g.95361415A= | GRCh37 |
NC_000010.9:g.95351405A= | NCBI36 |
NG_009104.1:g.4579T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371467.5:c.-315T= (RBP4) | ENSP00000360522.1:n.-315T= | |
ENST00000371469.2:c.51+8T= (RBP4) | ENSP00000360524.2:n.51+8T= | |
ENST00000604414.1:c.697-2416A= (FFAR4) | ENSP00000474477.1:n.697-2416A= | |
ENST00000629763.2:c.47+12T= (RBP4) | ENSP00000487033.1:n.47+12T= | |
NM_001323518.1:c.51+8T= (RBP4) | NP_001310447.1:n.51+8T= | |
NM_001323518.2:c.51+8T= (RBP4) | NP_001310447.1:n.51+8T= |