HGVS | Genome Assembly |
---|---|
NC_000010.11:g.119672424A>G , CM000672.2:g.119672424A>G | GRCh38 |
NC_000010.10:g.121431936A>G , CM000672.1:g.121431936A>G | GRCh37 |
NC_000010.9:g.121421926A>G | NCBI36 |
NG_016125.1:g.26055A>G , LRG_742:g.26055A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369085.8:c.677A>G MANE Select | ENSP00000358081.4:p.His226Arg | |
ENST00000369085.7:c.677A>G | ENSP00000358081.3:p.His226Arg | |
ENST00000450186.1:c.503A>G | ENSP00000410036.1:p.His168Arg | |
NM_004281.3:c.677A>G , LRG_742t1:c.677A>G | NP_004272.2:p.His226Arg | |
XM_005270287.1:c.677A>G | XP_005270344.1:p.His226Arg | |
XM_005270287.2:c.677A>G | XP_005270344.1:p.His226Arg | |
NM_004281.4:c.677A>G MANE Select | NP_004272.2:p.His226Arg |