HGVS | Genome Assembly |
---|---|
NC_000005.10:g.55233194C= , CM000667.2:g.55233194C= | GRCh38 |
NC_000005.9:g.54529022C= , CM000667.1:g.54529022C= | GRCh37 |
NC_000005.8:g.54564779C= | NCBI36 |
NG_034201.1:g.5524G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282572.5:c.330G= MANE Select | ENSP00000282572.4:p.Lys110= | |
ENST00000282572.4:c.330G= | ENSP00000282572.4:p.Lys110= | |
ENST00000501463.2:c.330G= | ENSP00000422485.1:p.Lys110= | |
NM_021147.4:c.330G= | NP_066970.3:p.Lys110= | |
NR_125346.1:n.524G= | ||
NR_125347.1:n.524G= | ||
NM_021147.5:c.330G= MANE Select | NP_066970.3:p.Lys110= | |
NR_125346.2:n.415G= | ||
NR_125347.2:n.415G= |