HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3225503T>A , CM000668.2:g.3225503T>A | GRCh38 |
NC_000006.11:g.3225737T>A , CM000668.1:g.3225737T>A | GRCh37 |
NC_000006.10:g.3170736T>A | NCBI36 |
NG_016715.1:g.7232A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259818.8:c.586A>T MANE Select | ENSP00000259818.6:p.Thr196Ser | |
ENST00000680070.1:n.1516A>T | ||
ENST00000681707.1:n.1413A>T | ||
ENST00000681757.1:n.891A>T | ||
ENST00000259818.7:c.586A>T | ENSP00000259818.6:p.Thr196Ser | |
ENST00000473006.1:n.703A>T | ||
NM_178012.4:c.586A>T | NP_821080.1:p.Thr196Ser | |
XM_011514571.1:c.370A>T | XP_011512873.1:p.Thr124Ser | |
NM_178012.5:c.586A>T MANE Select | NP_821080.1:p.Thr196Ser |