HGVS | Genome Assembly |
---|---|
NC_000010.11:g.119676609C>A , CM000672.2:g.119676609C>A | GRCh38 |
NC_000010.10:g.121436121C>A , CM000672.1:g.121436121C>A | GRCh37 |
NC_000010.9:g.121426111C>A | NCBI36 |
NG_016125.1:g.30240C>A , LRG_742:g.30240C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369085.8:c.1055C>A MANE Select | ENSP00000358081.4:p.Ser352Tyr | |
ENST00000369085.7:c.1055C>A | ENSP00000358081.3:p.Ser352Tyr | |
ENST00000450186.1:c.878C>A | ENSP00000410036.1:p.Ser293Tyr | |
NM_004281.3:c.1055C>A , LRG_742t1:c.1055C>A | NP_004272.2:p.Ser352Tyr | |
XM_005270287.1:c.1052C>A | XP_005270344.1:p.Ser351Tyr | |
XM_005270287.2:c.1052C>A | XP_005270344.1:p.Ser351Tyr | |
NM_004281.4:c.1055C>A MANE Select | NP_004272.2:p.Ser352Tyr |