HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31271328T= , CM000668.2:g.31271328T= | GRCh38 |
NC_000006.11:g.31239105T= , CM000668.1:g.31239105T= | GRCh37 |
NC_000006.10:g.31347084T= | NCBI36 |
NG_029422.2:g.5804A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376228.10:c.364A= MANE Select | ENSP00000365402.5:p.Met122= | |
ENST00000376228.9:c.364A= | ENSP00000365402.5:p.Met122= | |
ENST00000376237.8:c.347A= | ENSP00000365412.4:p.Asp116= | |
ENST00000383329.7:c.364A= | ENSP00000372819.3:p.Met122= | |
ENST00000415537.1:c.362A= | ||
ENST00000484378.1:n.633A= | ||
ENST00000487245.5:n.723A= | ||
ENST00000495835.1:n.553A= | ||
NM_002117.5:c.364A= | NP_002108.4:p.Met122= | |
NM_002117.6:c.364A= MANE Select | NP_002108.4:p.Met122= |