HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87709211T>A , CM000672.2:g.87709211T>A | GRCh38 |
NC_000010.10:g.89468968T>A , CM000672.1:g.89468968T>A | GRCh37 |
NC_000010.9:g.89458948T>A | NCBI36 |
NG_012150.1:g.54493T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000456849.2:c.43T>A MANE Select | ENSP00000406157.1:p.Ser15Thr | |
ENST00000361175.8:c.43T>A | ENSP00000354436.4:p.Ser15Thr | |
ENST00000456849.1:c.43T>A | ENSP00000406157.1:p.Ser15Thr | |
ENST00000465996.5:n.65T>A | ||
ENST00000482258.1:n.86T>A | ||
NM_001015880.1:c.43T>A | NP_001015880.1:p.Ser15Thr | |
NM_004670.3:c.43T>A | NP_004661.2:p.Ser15Thr | |
NM_001015880.2:c.43T>A MANE Select | NP_001015880.1:p.Ser15Thr | |
NM_004670.4:c.43T>A | NP_004661.2:p.Ser15Thr |