HGVS | Genome Assembly |
---|---|
NC_000005.10:g.55233325C>G , CM000667.2:g.55233325C>G | GRCh38 |
NC_000005.9:g.54529153C>G , CM000667.1:g.54529153C>G | GRCh37 |
NC_000005.8:g.54564910C>G | NCBI36 |
NG_034201.1:g.5393G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282572.5:c.199G>C MANE Select | ENSP00000282572.4:p.Gly67Arg | |
ENST00000282572.4:c.199G>C | ENSP00000282572.4:p.Gly67Arg | |
ENST00000501463.2:c.199G>C | ENSP00000422485.1:p.Gly67Arg | |
NM_021147.4:c.199G>C | NP_066970.3:p.Gly67Arg | |
NR_125346.1:n.393G>C | ||
NR_125347.1:n.393G>C | ||
NM_021147.5:c.199G>C MANE Select | NP_066970.3:p.Gly67Arg | |
NR_125346.2:n.284G>C | ||
NR_125347.2:n.284G>C |