HGVS | Genome Assembly |
---|---|
NC_000016.10:g.81365471T>A , CM000678.2:g.81365471T>A | GRCh38 |
NC_000016.9:g.81399076T>A , CM000678.1:g.81399076T>A | GRCh37 |
NC_000016.8:g.79956577T>A | NCBI36 |
NG_009007.1:g.55506T>A , LRG_242:g.55506T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648349.2:c.*1203T>A | ENSP00000498114.1:n.*1203T>A | |
ENST00000648994.2:c.1495T>A MANE Select | ENSP00000497351.1:p.Phe499Ile | |
ENST00000650388.1:c.1029T>A | ENSP00000498081.1:n.1029T>A | |
ENST00000567335.1:n.53T>A | ||
ENST00000568107.2:c.1495T>A | ENSP00000476795.1:p.Phe499Ile | |
NM_022041.3:c.1495T>A , LRG_242t1:c.1495T>A | NP_071324.1:p.Phe499Ile | |
XM_017023734.1:c.856T>A | XP_016879223.1:p.Phe286Ile | |
NM_001377486.1:c.856T>A | NP_001364415.1:p.Phe286Ile | |
NM_022041.4:c.1495T>A MANE Select | NP_071324.1:p.Phe499Ile |