HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42536645A>T , CM000679.2:g.42536645A>T | GRCh38 |
NC_000017.10:g.40688663A>T , CM000679.1:g.40688663A>T | GRCh37 |
NC_000017.9:g.37942189A>T | NCBI36 |
NG_011552.1:g.5713A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000225927.7:c.373A>T MANE Select | ENSP00000225927.1:p.Thr125Ser | |
ENST00000225927.6:c.373A>T | ENSP00000225927.1:p.Thr125Ser | |
ENST00000586516.5:c.123A>T | ||
ENST00000591587.1:c.116A>T | ENSP00000467836.1:p.His39Leu | |
NM_000263.3:c.373A>T | NP_000254.2:p.Thr125Ser | |
XM_006721920.2:c.-370A>T | XP_006721983.1:n.-370A>T | |
XM_011524840.1:c.-370A>T | XP_011523142.1:n.-370A>T | |
XM_024450771.1:c.373A>T | XP_024306539.1:p.Thr125Ser | |
NM_000263.4:c.373A>T MANE Select | NP_000254.2:p.Thr125Ser |