HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3225563A>T , CM000668.2:g.3225563A>T | GRCh38 |
NC_000006.11:g.3225797A>T , CM000668.1:g.3225797A>T | GRCh37 |
NC_000006.10:g.3170796A>T | NCBI36 |
NG_016715.1:g.7172T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000259818.8:c.526T>A MANE Select | ENSP00000259818.6:p.Ser176Thr | |
ENST00000680070.1:n.1456T>A | ||
ENST00000681707.1:n.1353T>A | ||
ENST00000681757.1:n.831T>A | ||
ENST00000259818.7:c.526T>A | ENSP00000259818.6:p.Ser176Thr | |
ENST00000473006.1:n.643T>A | ||
NM_178012.4:c.526T>A | NP_821080.1:p.Ser176Thr | |
XM_011514571.1:c.310T>A | XP_011512873.1:p.Ser104Thr | |
NM_178012.5:c.526T>A MANE Select | NP_821080.1:p.Ser176Thr |