HGVS | Genome Assembly |
---|---|
NC_000010.11:g.119672292C= , CM000672.2:g.119672292C= | GRCh38 |
NC_000010.10:g.121431804C= , CM000672.1:g.121431804C= | GRCh37 |
NC_000010.9:g.121421794C= | NCBI36 |
NG_016125.1:g.25923C= , LRG_742:g.25923C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369085.8:c.545C= MANE Select | ENSP00000358081.4:p.Ser182= | |
ENST00000369085.7:c.545C= | ENSP00000358081.3:p.Ser182= | |
ENST00000450186.1:c.371C= | ENSP00000410036.1:p.Ser124= | |
NM_004281.3:c.545C= , LRG_742t1:c.545C= | NP_004272.2:p.Ser182= | |
XM_005270287.1:c.545C= | XP_005270344.1:p.Ser182= | |
XM_005270287.2:c.545C= | XP_005270344.1:p.Ser182= | |
NM_004281.4:c.545C= MANE Select | NP_004272.2:p.Ser182= |