HGVS | Genome Assembly |
---|---|
NC_000005.10:g.135446767A= , CM000667.2:g.135446767A= | GRCh38 |
NC_000005.9:g.134782457A= , CM000667.1:g.134782457A= | GRCh37 |
NC_000005.8:g.134810356A= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000537858.2:c.*2687T= (TIFAB) MANE Select | ENSP00000440509.1:n.*2687T= | |
ENST00000503143.3:c.342T= (DCANP1) MANE Select | ENSP00000421871.1:p.His114= | |
ENST00000537858.1:c.*2687T= (TIFAB) | ENSP00000440509.1:n.*2687T= | |
NM_130848.2:c.342T= (DCANP1) | NP_570900.1:p.His114= | |
NM_001099221.2:c.*2687T= (TIFAB) MANE Select | NP_001092691.1:n.*2687T= | |
NM_130848.3:c.342T= (DCANP1) MANE Select | NP_570900.1:p.His114= |