HGVS | Genome Assembly |
---|---|
NC_000004.12:g.68670640T= , CM000666.2:g.68670640T= | GRCh38 |
NC_000004.11:g.69536358T= , CM000666.1:g.69536358T= | GRCh37 |
NC_000004.10:g.69218953T= | NCBI36 |
NG_052676.1:g.5137A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000338206.6:c.-22A= MANE Select | ENSP00000341045.5:n.-22A= | |
NM_001076.3:c.-22A= | NP_001067.2:n.-22A= | |
NM_001076.4:c.-22A= MANE Select | NP_001067.2:n.-22A= |