HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1213524T= , CM000667.2:g.1213524T= | GRCh38 |
NC_000005.9:g.1213639T= , CM000667.1:g.1213639T= | GRCh37 |
NC_000005.8:g.1266639T= | NCBI36 |
NG_008282.1:g.16930T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000304460.11:c.725T= MANE Select | ENSP00000305302.10:p.Leu242= | |
ENST00000304460.10:c.725T= | ENSP00000305302.10:p.Leu242= | |
ENST00000515652.5:c.633T= | ENSP00000425701.1:p.Pro211= | |
NM_001003841.2:c.725T= | NP_001003841.1:p.Leu242= | |
NM_001003841.3:c.725T= MANE Select | NP_001003841.1:p.Leu242= |