HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4898756C>T , CM000679.2:g.4898756C>T | GRCh38 |
NC_000017.10:g.4802051C>T , CM000679.1:g.4802051C>T | GRCh37 |
NC_000017.9:g.4742830C>T | NCBI36 |
NG_008029.2:g.9320G>A | |
NG_028005.1:g.70417C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000649488.2:c.1462G>A MANE Select | ENSP00000497829.1:p.Ala488Thr | |
ENST00000649830.1:c.*98G>A | ENSP00000496907.1:n.*98G>A | |
ENST00000652550.1:n.1188G>A | ||
ENST00000293780.4:c.1462G>A | ENSP00000293780.4:p.Ala488Thr | |
ENST00000572438.1:n.1148G>A | ||
NM_000080.3:c.1462G>A | NP_000071.1:p.Ala488Thr | |
NM_000080.4:c.1462G>A MANE Select | NP_000071.1:p.Ala488Thr | |
XM_017024115.1:c.1426G>A | XP_016879604.1:p.Ala476Thr |