HGVS | Genome Assembly |
---|---|
NC_000002.12:g.84425558C>T , CM000664.2:g.84425558C>T | GRCh38 |
NC_000002.11:g.84652682C>T , CM000664.1:g.84652682C>T | GRCh37 |
NC_000002.10:g.84506193C>T | NCBI36 |
NG_016755.1:g.38905G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000393868.7:c.871G>A MANE Select | ENSP00000377446.2:p.Ala291Thr | |
ENST00000651342.1:c.*311G>A | ENSP00000498471.1:n.*311G>A | |
ENST00000393868.6:c.871G>A | ENSP00000377446.2:p.Ala291Thr | |
ENST00000484365.1:n.1379G>A | ||
ENST00000487809.1:n.618G>A | ||
ENST00000491123.5:n.717G>A | ||
NM_003849.3:c.871G>A | NP_003840.2:p.Ala291Thr | |
NM_003849.4:c.871G>A MANE Select | NP_003840.2:p.Ala291Thr |