HGVS | Genome Assembly |
---|---|
NC_000003.12:g.49125463C= , CM000665.2:g.49125463C= | GRCh38 |
NC_000003.11:g.49162896C= , CM000665.1:g.49162896C= | GRCh37 |
NC_000003.10:g.49137900C= | NCBI36 |
NG_008094.1:g.12704G= | |
NG_054716.1:g.476G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305544.9:c.2510G= MANE Select | ENSP00000307156.4:p.Gly837= | |
ENST00000305544.8:c.2510G= | ENSP00000307156.4:p.Gly837= | |
ENST00000418109.5:c.2510G= | ENSP00000388325.1:p.Gly837= | |
ENST00000464891.5:n.259G= | ||
ENST00000477701.1:n.383G= | ||
ENST00000483057.1:n.110G= | ||
ENST00000486298.5:n.426-294G= | ||
NM_002292.3:c.2510G= | NP_002283.3:p.Gly837= | |
XM_005265127.3:c.2510G= | XP_005265184.1:p.Gly837= | |
XM_005265127.4:c.2510G= | XP_005265184.1:p.Gly837= | |
NM_002292.4:c.2510G= MANE Select | NP_002283.3:p.Gly837= |