HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17022721A>G , CM000663.2:g.17022721A>G | GRCh38 |
NC_000001.10:g.17349216A>G , CM000663.1:g.17349216A>G | GRCh37 |
NC_000001.9:g.17221803A>G | NCBI36 |
NG_012340.1:g.36450T>C , LRG_316:g.36450T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000463045.3:c.481T>C | ENSP00000481376.2:p.Trp161Arg | |
ENST00000491274.6:c.610T>C | ENSP00000480482.2:p.Trp204Arg | |
ENST00000375499.8:c.652T>C MANE Select | ENSP00000364649.3:p.Trp218Arg | |
ENST00000375499.7:c.652T>C | ENSP00000364649.3:p.Trp218Arg | |
ENST00000475049.5:n.77T>C | ||
ENST00000485092.5:n.316T>C | ||
ENST00000485515.5:n.586T>C | ||
NM_003000.2:c.652T>C , LRG_316t1:c.652T>C | NP_002991.2:p.Trp218Arg | |
NM_003000.3:c.652T>C MANE Select | NP_002991.2:p.Trp218Arg |