HGVS | Genome Assembly |
---|---|
NC_000016.10:g.81315265C>A , CM000678.2:g.81315265C>A | GRCh38 |
NC_000016.9:g.81348870C>A , CM000678.1:g.81348870C>A | GRCh37 |
NC_000016.8:g.79906371C>A | NCBI36 |
NG_009007.1:g.5300C>A , LRG_242:g.5300C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648349.2:c.152C>A | ENSP00000498114.1:p.Ala51Asp | |
ENST00000648994.2:c.152C>A MANE Select | ENSP00000497351.1:p.Ala51Asp | |
ENST00000650388.1:c.152C>A | ENSP00000498081.1:p.Ala51Asp | |
ENST00000674788.1:n.277C>A | ||
ENST00000568107.2:c.152C>A | ENSP00000476795.1:p.Ala51Asp | |
NM_022041.3:c.152C>A , LRG_242t1:c.152C>A | NP_071324.1:p.Ala51Asp | |
XM_017023734.1:c.-373C>A | XP_016879223.1:n.-373C>A | |
NM_001377486.1:c.-373C>A | NP_001364415.1:n.-373C>A | |
NM_022041.4:c.152C>A MANE Select | NP_071324.1:p.Ala51Asp |