HGVS | Genome Assembly |
---|---|
NC_000007.14:g.147132368A= , CM000669.2:g.147132368A= | GRCh38 |
NC_000007.13:g.146829460A= , CM000669.1:g.146829460A= | GRCh37 |
NC_000007.12:g.146460393A= | NCBI36 |
NG_007092.2:g.1021008A= | |
NG_007092.3:g.1021368A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361727.8:c.1207A= MANE Select | ENSP00000354778.3:p.Thr403= | |
ENST00000636561.1:n.1110A= | ||
ENST00000636870.1:n.1069A= | ||
ENST00000637150.1:n.1136A= | ||
ENST00000637694.1:n.1110A= | ||
ENST00000637825.1:n.690A= | ||
ENST00000638117.1:n.1110A= | ||
ENST00000361727.7:c.1207A= | ENSP00000354778.3:p.Thr403= | |
NM_014141.5:c.1207A= | NP_054860.1:p.Thr403= | |
XM_017011950.2:c.1207A= | XP_016867439.1:p.Thr403= | |
NM_014141.6:c.1207A= MANE Select | NP_054860.1:p.Thr403= |