HGVS | Genome Assembly |
---|---|
NC_000010.11:g.30313900T>C , CM000672.2:g.30313900T>C | GRCh38 |
NC_000010.10:g.30602829T>C , CM000672.1:g.30602829T>C | GRCh37 |
NC_000010.9:g.30642835T>C | NCBI36 |
NG_028096.1:g.40439A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263063.9:c.1458A>G MANE Select | ENSP00000263063.3:p.Ile486Met | |
ENST00000263063.8:c.1458A>G | ENSP00000263063.3:p.Ile486Met | |
ENST00000488290.5:n.3213A>G | ||
NM_018109.3:c.1458A>G | NP_060579.3:p.Ile486Met | |
NM_018109.4:c.1458A>G MANE Select | NP_060579.3:p.Ile486Met |