HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94111526C>G , CM000663.2:g.94111526C>G | GRCh38 |
NC_000001.10:g.94577082C>G , CM000663.1:g.94577082C>G | GRCh37 |
NC_000001.9:g.94349670C>G | NCBI36 |
NG_009073.1:g.14624G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.214G>C MANE Select | ENSP00000359245.3:p.Gly72Arg | |
ENST00000649773.1:c.214G>C | ENSP00000496882.1:p.Gly72Arg | |
ENST00000370225.3:c.214G>C | ENSP00000359245.3:p.Gly72Arg | |
NM_000350.2:c.214G>C | NP_000341.2:p.Gly72Arg | |
NM_000350.3:c.214G>C MANE Select | NP_000341.2:p.Gly72Arg |