HGVS | Genome Assembly |
---|---|
NC_000004.12:g.68646952A= , CM000666.2:g.68646952A= | GRCh38 |
NC_000004.11:g.69512670A= , CM000666.1:g.69512670A= | GRCh37 |
NC_000004.10:g.69195265A= | NCBI36 |
NG_052676.1:g.28825T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000338206.6:c.*152T= MANE Select | ENSP00000341045.5:n.*152T= | |
ENST00000338206.5:c.*152T= | ENSP00000341045.5:n.*152T= | |
ENST00000616841.4:c.1732+13T= | ENSP00000482004.1:n.1732+13T= | |
NM_001076.3:c.*152T= | NP_001067.2:n.*152T= | |
NM_001076.4:c.*152T= MANE Select | NP_001067.2:n.*152T= |