HGVS | Genome Assembly |
---|---|
NC_000010.11:g.93601643C= , CM000672.2:g.93601643C= | GRCh38 |
NC_000010.10:g.95361400C= , CM000672.1:g.95361400C= | GRCh37 |
NC_000010.9:g.95351390C= | NCBI36 |
NG_009104.1:g.4594G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371467.5:c.-300G= (RBP4) | ENSP00000360522.1:n.-300G= | |
ENST00000371469.2:c.51+23G= (RBP4) | ENSP00000360524.2:n.51+23G= | |
ENST00000604414.1:c.697-2431C= (FFAR4) | ENSP00000474477.1:n.697-2431C= | |
ENST00000629763.2:c.47+27G= (RBP4) | ENSP00000487033.1:n.47+27G= | |
NM_001323518.1:c.51+23G= (RBP4) | NP_001310447.1:n.51+23G= | |
NM_001323518.2:c.51+23G= (RBP4) | NP_001310447.1:n.51+23G= |