HGVS | Genome Assembly |
---|---|
NC_000005.10:g.148827336A>T , CM000667.2:g.148827336A>T | GRCh38 |
NC_000005.9:g.148206899A>T , CM000667.1:g.148206899A>T | GRCh37 |
NC_000005.8:g.148187092A>T | NCBI36 |
NG_016421.1:g.5744A>T | |
NG_016421.2:g.5744A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305988.6:c.505A>T MANE Select | ENSP00000305372.4:p.Ile169Phe | |
ENST00000305988.5:c.505A>T | ENSP00000305372.4:p.Ile169Phe | |
NM_000024.5:c.505A>T | NP_000015.1:p.Ile169Phe | |
NM_000024.6:c.505A>T MANE Select | NP_000015.2:p.Ile169Phe |