HGVS | Genome Assembly |
---|---|
NC_000010.11:g.133538822T>G , CM000672.2:g.133538822T>G | GRCh38 |
NC_000010.10:g.135352326T>G , CM000672.1:g.135352326T>G | GRCh37 |
NC_000010.9:g.135202316T>G | NCBI36 |
NG_008383.1:g.16460T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252945.8:c.1340T>G MANE Select | ENSP00000252945.3:p.Leu447Trp | |
ENST00000252945.7:c.1340T>G | ENSP00000252945.3:p.Leu447Trp | |
ENST00000368520.1:n.1358+930T>G | ||
ENST00000463117.6:c.1340T>G | ENSP00000440689.1:p.Leu447Trp | |
ENST00000469258.1:n.436T>G | ||
NM_000773.3:c.1340T>G | NP_000764.1:p.Leu447Trp | |
NM_000773.4:c.1340T>G MANE Select | NP_000764.1:p.Leu447Trp |