HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136659159T>C , CM000685.2:g.136659159T>C | GRCh38 |
NC_000023.10:g.135741318T>C , CM000685.1:g.135741318T>C | GRCh37 |
NC_000023.9:g.135568984T>C | NCBI36 |
NG_007280.1:g.15983T>C , LRG_141:g.15983T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695724.1:c.*148T>C | ENSP00000512122.1:n.*148T>C | |
ENST00000695725.1:c.*85T>C | ENSP00000512123.1:n.*85T>C | |
ENST00000695726.1:n.2498T>C | ||
ENST00000695729.1:n.3333T>C | ||
ENST00000370629.7:c.530T>C MANE Select | ENSP00000359663.2:p.Phe177Ser | |
ENST00000370628.2:c.467T>C | ENSP00000359662.2:p.Phe156Ser | |
ENST00000370629.6:c.530T>C | ENSP00000359663.2:p.Phe177Ser | |
NM_000074.2:c.530T>C , LRG_141t1:c.530T>C | NP_000065.1:p.Phe177Ser | |
NM_000074.3:c.530T>C MANE Select | NP_000065.1:p.Phe177Ser |