HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5226827C= , CM000673.2:g.5226827C= | GRCh38 |
NC_000011.9:g.5248057C= , CM000673.1:g.5248057C= | GRCh37 |
NC_000011.8:g.5204633C= | NCBI36 |
NG_000007.3:g.70789G= | |
NG_059281.1:g.5245G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647020.1:c.93-28G= | ENSP00000494175.1:n.93-28G= | |
ENST00000335295.4:c.93-28G= MANE Select | ENSP00000333994.3:n.93-28G= | |
ENST00000380315.2:c.93-28G= | ENSP00000369671.2:n.93-28G= | |
ENST00000485743.1:n.144-28G= | ||
ENST00000633227.1:c.77-28G= | ENSP00000488004.1:n.77-28G= | |
NM_000518.4:c.93-28G= | NP_000509.1:n.93-28G= | |
NM_000518.5:c.93-28G= MANE Select | NP_000509.1:n.93-28G= |