HGVS | Genome Assembly |
---|---|
NC_000004.12:g.68670166T= , CM000666.2:g.68670166T= | GRCh38 |
NC_000004.11:g.69535884T= , CM000666.1:g.69535884T= | GRCh37 |
NC_000004.10:g.69218479T= | NCBI36 |
NG_052676.1:g.5611A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000338206.6:c.453A= MANE Select | ENSP00000341045.5:p.Ala151= | |
ENST00000338206.5:c.453A= | ENSP00000341045.5:p.Ala151= | |
ENST00000616841.4:c.453A= | ENSP00000482004.1:p.Ala151= | |
NM_001076.3:c.453A= | NP_001067.2:p.Ala151= | |
NM_001076.4:c.453A= MANE Select | NP_001067.2:p.Ala151= |