HGVS | Genome Assembly |
---|---|
NC_000011.10:g.62576911T= , CM000673.2:g.62576911T= | GRCh38 |
NC_000011.9:g.62344383T= , CM000673.1:g.62344383T= | GRCh37 |
NC_000011.8:g.62100959T= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000476907.6:c.1377A= MANE Select | ENSP00000419607.1:p.Lys459= | |
ENST00000308436.11:c.1491A= | ENSP00000308000.7:p.Lys497= | |
ENST00000463241.2:n.242A= | ||
ENST00000469480.1:n.183A= | ||
ENST00000476907.5:c.1377A= | ENSP00000419607.1:p.Lys459= | |
ENST00000496634.2:c.1377A= | ENSP00000456163.1:p.Lys459= | |
ENST00000526409.5:n.247A= | ||
NM_022830.2:c.1491A= | NP_073741.2:p.Lys497= | |
NM_001367906.1:c.1318A= | NP_001354835.1:p.Ser440= | |
NM_022830.3:c.1377A= MANE Select | NP_073741.3:p.Lys459= |