HGVS | Genome Assembly |
---|---|
NC_000005.10:g.55233192G>C , CM000667.2:g.55233192G>C | GRCh38 |
NC_000005.9:g.54529020G>C , CM000667.1:g.54529020G>C | GRCh37 |
NC_000005.8:g.54564777G>C | NCBI36 |
NG_034201.1:g.5526C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282572.5:c.332C>G MANE Select | ENSP00000282572.4:p.Ala111Gly | |
ENST00000282572.4:c.332C>G | ENSP00000282572.4:p.Ala111Gly | |
ENST00000501463.2:c.332C>G | ENSP00000422485.1:p.Ala111Gly | |
NM_021147.4:c.332C>G | NP_066970.3:p.Ala111Gly | |
NR_125346.1:n.526C>G | ||
NR_125347.1:n.526C>G | ||
NM_021147.5:c.332C>G MANE Select | NP_066970.3:p.Ala111Gly | |
NR_125346.2:n.417C>G | ||
NR_125347.2:n.417C>G |