HGVS | Genome Assembly |
---|---|
NC_000010.11:g.119672553C>A , CM000672.2:g.119672553C>A | GRCh38 |
NC_000010.10:g.121432065C>A , CM000672.1:g.121432065C>A | GRCh37 |
NC_000010.9:g.121422055C>A | NCBI36 |
NG_016125.1:g.26184C>A , LRG_742:g.26184C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369085.8:c.806C>A MANE Select | ENSP00000358081.4:p.Ser269Tyr | |
ENST00000369085.7:c.806C>A | ENSP00000358081.3:p.Ser269Tyr | |
ENST00000450186.1:c.632C>A | ENSP00000410036.1:p.Ser211Tyr | |
NM_004281.3:c.806C>A , LRG_742t1:c.806C>A | NP_004272.2:p.Ser269Tyr | |
XM_005270287.1:c.806C>A | XP_005270344.1:p.Ser269Tyr | |
XM_005270287.2:c.806C>A | XP_005270344.1:p.Ser269Tyr | |
NM_004281.4:c.806C>A MANE Select | NP_004272.2:p.Ser269Tyr |