HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136659102G>C , CM000685.2:g.136659102G>C | GRCh38 |
NC_000023.10:g.135741261G>C , CM000685.1:g.135741261G>C | GRCh37 |
NC_000023.9:g.135568927G>C | NCBI36 |
NG_007280.1:g.15926G>C , LRG_141:g.15926G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000695724.1:c.*91G>C | ENSP00000512122.1:n.*91G>C | |
ENST00000695725.1:c.*28G>C | ENSP00000512123.1:n.*28G>C | |
ENST00000695726.1:n.2441G>C | ||
ENST00000695729.1:n.3276G>C | ||
ENST00000370629.7:c.473G>C MANE Select | ENSP00000359663.2:p.Gly158Ala | |
ENST00000370628.2:c.410G>C | ENSP00000359662.2:p.Gly137Ala | |
ENST00000370629.6:c.473G>C | ENSP00000359663.2:p.Gly158Ala | |
NM_000074.2:c.473G>C , LRG_141t1:c.473G>C | NP_000065.1:p.Gly158Ala | |
NM_000074.3:c.473G>C MANE Select | NP_000065.1:p.Gly158Ala |