HGVS | Genome Assembly |
---|---|
NC_000011.10:g.116832871C>A , CM000673.2:g.116832871C>A | GRCh38 |
NC_000011.9:g.116703587C>A , CM000673.1:g.116703587C>A | GRCh37 |
NC_000011.8:g.116208797C>A | NCBI36 |
NG_008949.1:g.7964C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000227667.8:c.287C>A MANE Select | ENSP00000227667.2:p.Ala96Asp | |
ENST00000227667.7:c.287C>A | ENSP00000227667.2:p.Ala96Asp | |
ENST00000375345.3:c.341C>A | ENSP00000364494.1:p.Ala114Asp | |
ENST00000630701.1:c.341C>A | ENSP00000486182.1:p.Ala114Asp | |
NM_000040.1:c.287C>A | NP_000031.1:p.Ala96Asp | |
NM_000040.2:c.287C>A | NP_000031.1:p.Ala96Asp | |
NM_000040.3:c.287C>A MANE Select | NP_000031.1:p.Ala96Asp |