HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91055939C>G , CM000674.2:g.91055939C>G | GRCh38 |
NC_000012.11:g.91449716C>G , CM000674.1:g.91449716C>G | GRCh37 |
NC_000012.10:g.89973847C>G | NCBI36 |
NG_021223.1:g.7416G>C , LRG_538:g.7416G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266719.4:c.343G>C MANE Select | ENSP00000266719.3:p.Gly115Arg | |
ENST00000266719.3:c.343G>C | ENSP00000266719.3:p.Gly115Arg | |
NM_007035.3:c.343G>C , LRG_538t1:c.343G>C | NP_008966.1:p.Gly115Arg | |
XM_011537781.1:c.343G>C | XP_011536083.1:p.Gly115Arg | |
NM_007035.4:c.343G>C MANE Select | NP_008966.1:p.Gly115Arg |