HGVS | Genome Assembly |
---|---|
NC_000007.14:g.155811898T>A , CM000669.2:g.155811898T>A | GRCh38 |
NC_000007.13:g.155604592T>A , CM000669.1:g.155604592T>A | GRCh37 |
NC_000007.12:g.155297353T>A | NCBI36 |
NG_007504.2:g.5376A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297261.7:c.225A>T MANE Select | ENSP00000297261.2:p.Glu75Asp | |
ENST00000297261.6:c.225A>T | ENSP00000297261.2:p.Glu75Asp | |
NM_000193.2:c.225A>T | NP_000184.1:p.Glu75Asp | |
NM_000193.3:c.225A>T | NP_000184.1:p.Glu75Asp | |
NM_000193.4:c.225A>T MANE Select | NP_000184.1:p.Glu75Asp |