HGVS | Genome Assembly |
---|---|
NC_000005.10:g.55233287A= , CM000667.2:g.55233287A= | GRCh38 |
NC_000005.9:g.54529115A= , CM000667.1:g.54529115A= | GRCh37 |
NC_000005.8:g.54564872A= | NCBI36 |
NG_034201.1:g.5431T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282572.5:c.237T= MANE Select | ENSP00000282572.4:p.Gly79= | |
ENST00000282572.4:c.237T= | ENSP00000282572.4:p.Gly79= | |
ENST00000501463.2:c.237T= | ENSP00000422485.1:p.Gly79= | |
NM_021147.4:c.237T= | NP_066970.3:p.Gly79= | |
NR_125346.1:n.431T= | ||
NR_125347.1:n.431T= | ||
NM_021147.5:c.237T= MANE Select | NP_066970.3:p.Gly79= | |
NR_125346.2:n.322T= | ||
NR_125347.2:n.322T= |