HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17024013C>G , CM000663.2:g.17024013C>G | GRCh38 |
NC_000001.10:g.17350508C>G , CM000663.1:g.17350508C>G | GRCh37 |
NC_000001.9:g.17223095C>G | NCBI36 |
NG_012340.1:g.35158G>C , LRG_316:g.35158G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000463045.3:c.431G>C | ENSP00000481376.2:p.Trp144Ser | |
ENST00000491274.6:c.560G>C | ENSP00000480482.2:p.Trp187Ser | |
ENST00000375499.8:c.602G>C MANE Select | ENSP00000364649.3:p.Trp201Ser | |
ENST00000375499.7:c.602G>C | ENSP00000364649.3:p.Trp201Ser | |
ENST00000485515.5:n.536G>C | ||
ENST00000491274.5:c.560G>C | ENSP00000480482.1:p.Trp187Ser | |
NM_003000.2:c.602G>C , LRG_316t1:c.602G>C | NP_002991.2:p.Trp201Ser | |
NM_003000.3:c.602G>C MANE Select | NP_002991.2:p.Trp201Ser |