HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31634968G= , CM000668.2:g.31634968G= | GRCh38 |
NC_000006.11:g.31602745G= , CM000668.1:g.31602745G= | GRCh37 |
NC_000006.10:g.31710724G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376033.3:c.5151G= MANE Select | ENSP00000365201.2:p.Gly1717= | |
ENST00000376007.8:c.5151G= | ENSP00000365175.4:p.Gly1717= | |
ENST00000376033.2:c.5151G= | ENSP00000365201.2:p.Gly1717= | |
ENST00000484787.1:n.562G= | ||
NM_004638.3:c.5151G= | NP_004629.3:p.Gly1717= | |
NM_080686.2:c.5151G= | NP_542417.2:p.Gly1717= | |
XM_011514890.1:c.5151G= | XP_011513192.1:p.Gly1717= | |
XM_017011274.1:c.5151G= | XP_016866763.1:p.Gly1717= | |
NM_004638.4:c.5151G= MANE Select | NP_004629.3:p.Gly1717= | |
NM_080686.3:c.5151G= | NP_542417.2:p.Gly1717= |