HGVS | Genome Assembly |
---|---|
NC_000010.11:g.93601669C>G , CM000672.2:g.93601669C>G | GRCh38 |
NC_000010.10:g.95361426C>G , CM000672.1:g.95361426C>G | GRCh37 |
NC_000010.9:g.95351416C>G | NCBI36 |
NG_009104.1:g.4568G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371469.2:c.48G>C (RBP4) | ENSP00000360524.2:p.Thr16= | |
ENST00000604414.1:c.697-2405C>G (FFAR4) | ENSP00000474477.1:n.697-2405C>G | |
ENST00000629763.2:c.47+1G>C (RBP4) | ENSP00000487033.1:n.47+1G>C | |
NM_001323518.1:c.48G>C (RBP4) | NP_001310447.1:p.Thr16= | |
NM_001323518.2:c.48G>C (RBP4) | NP_001310447.1:p.Thr16= |