HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5226645T= , CM000673.2:g.5226645T= | GRCh38 |
NC_000011.9:g.5247875T= , CM000673.1:g.5247875T= | GRCh37 |
NC_000011.8:g.5204451T= | NCBI36 |
NG_000007.3:g.70971A= | |
NG_059281.1:g.5427A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647020.1:c.247A= | ENSP00000494175.1:p.Lys83= | |
ENST00000335295.4:c.247A= MANE Select | ENSP00000333994.3:p.Lys83= | |
ENST00000380315.2:c.247A= | ENSP00000369671.2:p.Lys83= | |
ENST00000475226.1:n.179A= | ||
ENST00000485743.1:n.298A= | ||
ENST00000633227.1:c.*63A= | ENSP00000488004.1:n.*63A= | |
NM_000518.4:c.247A= | NP_000509.1:p.Lys83= | |
NM_000518.5:c.247A= MANE Select | NP_000509.1:p.Lys83= |