HGVS | Genome Assembly |
---|---|
NC_000011.10:g.299409C= , CM000673.2:g.299409C= | GRCh38 |
NC_000011.9:g.299409C= , CM000673.1:g.299409C= | GRCh37 |
NC_000011.8:g.289409C= | NCBI36 |
NG_032892.1:g.5118G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382614.2:c.82G= MANE Select | ENSP00000372059.2:p.Ala28= | |
NM_001025295.2:c.82G= | NP_001020466.1:p.Ala28= | |
NM_001025295.3:c.82G= MANE Select | NP_001020466.1:p.Ala28= |