HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136659049G>C , CM000685.2:g.136659049G>C | GRCh38 |
NC_000023.10:g.135741208G>C , CM000685.1:g.135741208G>C | GRCh37 |
NC_000023.9:g.135568874G>C | NCBI36 |
NG_007280.1:g.15873G>C , LRG_141:g.15873G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695724.1:c.*38G>C | ENSP00000512122.1:n.*38G>C | |
ENST00000695725.1:c.167G>C | ENSP00000512123.1:p.Gly56Ala | |
ENST00000695726.1:n.2388G>C | ||
ENST00000695729.1:n.3223G>C | ||
ENST00000370629.7:c.420G>C MANE Select | ENSP00000359663.2:p.Trp140Cys | |
ENST00000370628.2:c.357G>C | ENSP00000359662.2:p.Trp119Cys | |
ENST00000370629.6:c.420G>C | ENSP00000359663.2:p.Trp140Cys | |
NM_000074.2:c.420G>C , LRG_141t1:c.420G>C | NP_000065.1:p.Trp140Cys | |
NM_000074.3:c.420G>C MANE Select | NP_000065.1:p.Trp140Cys |