HGVS | Genome Assembly |
---|---|
NC_000023.11:g.119930095G>T , CM000685.2:g.119930095G>T | GRCh38 |
NC_000023.10:g.119064058G>T , CM000685.1:g.119064058G>T | GRCh37 |
NC_000023.9:g.118948086G>T | NCBI36 |
NG_021260.1:g.18678C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371410.5:c.994C>A MANE Select | ENSP00000360464.3:p.Pro332Thr | |
ENST00000652253.1:c.990C>A | ||
ENST00000371410.4:c.994C>A | ENSP00000360464.3:p.Pro332Thr | |
ENST00000477789.5:n.1922C>A | ||
NM_024528.3:c.994C>A | NP_078804.2:p.Pro332Thr | |
XM_017029842.1:c.697C>A | XP_016885331.1:p.Pro233Thr | |
NM_024528.4:c.994C>A MANE Select | NP_078804.2:p.Pro332Thr |