HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154965978T>A , CM000685.2:g.154965978T>A | GRCh38 |
NC_000023.10:g.154194253T>A , CM000685.1:g.154194253T>A | GRCh37 |
NC_000023.9:g.153847447T>A | NCBI36 |
NG_011403.1:g.61746A>T | |
NG_011403.2:g.61746A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000360256.9:c.1435A>T MANE Select | ENSP00000353393.4:p.Thr479Ser | |
ENST00000647125.1:c.*1311A>T | ENSP00000496062.1:n.*1311A>T | |
ENST00000360256.8:c.1435A>T | ENSP00000353393.4:p.Thr479Ser | |
ENST00000483822.2:n.255A>T | ||
NM_000132.3:c.1435A>T | NP_000123.1:p.Thr479Ser | |
XM_011531126.1:c.1330A>T | XP_011529428.1:p.Thr444Ser | |
NM_000132.4:c.1435A>T MANE Select | NP_000123.1:p.Thr479Ser |