HGVS | Genome Assembly |
---|---|
NC_000004.12:g.68670629T= , CM000666.2:g.68670629T= | GRCh38 |
NC_000004.11:g.69536347T= , CM000666.1:g.69536347T= | GRCh37 |
NC_000004.10:g.69218942T= | NCBI36 |
NG_052676.1:g.5148A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000338206.6:c.-11A= MANE Select | ENSP00000341045.5:n.-11A= | |
NM_001076.3:c.-11A= | NP_001067.2:n.-11A= | |
NM_001076.4:c.-11A= MANE Select | NP_001067.2:n.-11A= |