HGVS | Genome Assembly |
---|---|
NC_000010.11:g.119669969A= , CM000672.2:g.119669969A= | GRCh38 |
NC_000010.10:g.121429481A= , CM000672.1:g.121429481A= | GRCh37 |
NC_000010.9:g.121419471A= | NCBI36 |
NG_016125.1:g.23600A= , LRG_742:g.23600A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369085.8:c.299A= MANE Select | ENSP00000358081.4:p.His100= | |
ENST00000369085.7:c.299A= | ENSP00000358081.3:p.His100= | |
ENST00000450186.1:c.125A= | ENSP00000410036.1:p.His42= | |
NM_004281.3:c.299A= , LRG_742t1:c.299A= | NP_004272.2:p.His100= | |
XM_005270287.1:c.299A= | XP_005270344.1:p.His100= | |
XM_005270287.2:c.299A= | XP_005270344.1:p.His100= | |
NM_004281.4:c.299A= MANE Select | NP_004272.2:p.His100= |