HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52519936C= , CM000674.2:g.52519936C= | GRCh38 |
NC_000012.11:g.52913720C= , CM000674.1:g.52913720C= | GRCh37 |
NC_000012.10:g.51199987C= | NCBI36 |
NG_008297.1:g.5524G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252242.9:c.361G= MANE Select | ENSP00000252242.4:p.Ala121= | |
ENST00000252242.8:c.361G= | ENSP00000252242.4:p.Ala121= | |
ENST00000546577.1:c.361G= | ENSP00000449651.1:p.Ala121= | |
ENST00000549420.1:c.44-13G= | ENSP00000447209.1:n.44-13G= | |
ENST00000551275.1:c.256G= | ENSP00000448041.1:p.Ala86= | |
ENST00000552629.5:n.459G= | ||
NM_000424.3:c.361G= | NP_000415.2:p.Ala121= | |
NM_000424.4:c.361G= MANE Select | NP_000415.2:p.Ala121= |