HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31270413C= , CM000668.2:g.31270413C= | GRCh38 |
NC_000006.11:g.31238190C= , CM000668.1:g.31238190C= | GRCh37 |
NC_000006.10:g.31346169C= | NCBI36 |
NG_029422.2:g.6719G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.692G= MANE Select | ENSP00000365402.5:p.Gly231= | |
ENST00000376228.9:c.692G= | ENSP00000365402.5:p.Gly231= | |
ENST00000376237.8:c.*279G= | ENSP00000365412.4:n.*279G= | |
ENST00000383329.7:c.692G= | ENSP00000372819.3:p.Gly231= | |
ENST00000415537.1:c.664+26G= | ||
ENST00000470363.5:n.10G= | ||
ENST00000487245.5:n.1051G= | ||
ENST00000495835.1:n.881G= | ||
NM_002117.5:c.692G= | NP_002108.4:p.Gly231= | |
NM_002117.6:c.692G= MANE Select | NP_002108.4:p.Gly231= |