HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52038139A= , CM000666.2:g.52038139A= | GRCh38 |
NC_000004.11:g.52904305A= , CM000666.1:g.52904305A= | GRCh37 |
NC_000004.10:g.52599062A= | NCBI36 |
NG_008891.1:g.5181T= , LRG_204:g.5181T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.10:c.33+88T= MANE Select | ENSP00000370839.6:n.33+88T= | |
ENST00000381431.9:c.33+88T= | ENSP00000370839.5:n.33+88T= | |
ENST00000506357.5:c.19+88T= | ||
NM_000232.4:c.33+88T= , LRG_204t1:c.33+88T= | NP_000223.1:n.33+88T= | |
XM_011534403.1:c.33+88T= | XP_011532705.1:n.33+88T= | |
NM_000232.5:c.33+88T= MANE Select | NP_000223.1:n.33+88T= |