HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31271255T= , CM000668.2:g.31271255T= | GRCh38 |
NC_000006.11:g.31239032T= , CM000668.1:g.31239032T= | GRCh37 |
NC_000006.10:g.31347011T= | NCBI36 |
NG_029422.2:g.5877A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376228.10:c.437A= MANE Select | ENSP00000365402.5:p.Asp146= | |
ENST00000376228.9:c.437A= | ENSP00000365402.5:p.Asp146= | |
ENST00000376237.8:c.*24A= | ENSP00000365412.4:n.*24A= | |
ENST00000383329.7:c.437A= | ENSP00000372819.3:p.Asp146= | |
ENST00000415537.1:c.435A= | ||
ENST00000484378.1:n.706A= | ||
ENST00000487245.5:n.796A= | ||
ENST00000495835.1:n.626A= | ||
NM_002117.5:c.437A= | NP_002108.4:p.Asp146= | |
NM_002117.6:c.437A= MANE Select | NP_002108.4:p.Asp146= |