HGVS | Genome Assembly |
---|---|
NC_000011.10:g.69648128A>T , CM000673.2:g.69648128A>T | GRCh38 |
NC_000011.9:g.69462896A>T , CM000673.1:g.69462896A>T | GRCh37 |
NC_000011.8:g.69172077A>T | NCBI36 |
NG_007375.1:g.12024A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000227507.3:c.709A>T MANE Select | ENSP00000227507.2:p.Ile237Phe | |
ENST00000227507.2:c.709A>T | ENSP00000227507.2:p.Ile237Phe | |
ENST00000536559.1:c.*129A>T | ENSP00000438482.1:n.*129A>T | |
ENST00000542367.1:n.172A>T | ||
ENST00000545484.1:n.415A>T | ||
NM_053056.2:c.709A>T | NP_444284.1:p.Ile237Phe | |
XM_006718653.2:c.733A>T | XP_006718716.1:p.Ile245Phe | |
NM_053056.3:c.709A>T MANE Select | NP_444284.1:p.Ile237Phe |