HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31271376T= , CM000668.2:g.31271376T= | GRCh38 |
NC_000006.11:g.31239153T= , CM000668.1:g.31239153T= | GRCh37 |
NC_000006.10:g.31347132T= | NCBI36 |
NG_029422.2:g.5756A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376228.10:c.344-28A= MANE Select | ENSP00000365402.5:n.344-28A= | |
ENST00000376228.9:c.344-28A= | ENSP00000365402.5:n.344-28A= | |
ENST00000376237.8:c.344-45A= | ENSP00000365412.4:n.344-45A= | |
ENST00000383329.7:c.344-28A= | ENSP00000372819.3:n.344-28A= | |
ENST00000415537.1:c.342-28A= | ||
ENST00000484378.1:n.585A= | ||
ENST00000487245.5:n.675A= | ||
ENST00000495835.1:n.533-28A= | ||
NM_002117.5:c.344-28A= | NP_002108.4:n.344-28A= | |
NM_002117.6:c.344-28A= MANE Select | NP_002108.4:n.344-28A= |