HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52033505A= , CM000666.2:g.52033505A= | GRCh38 |
NC_000004.11:g.52899671A= , CM000666.1:g.52899671A= | GRCh37 |
NC_000004.10:g.52594428A= | NCBI36 |
NG_008891.1:g.9815T= , LRG_204:g.9815T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.10:c.169T= MANE Select | ENSP00000370839.6:p.Leu57= | |
ENST00000381431.9:c.169T= | ENSP00000370839.5:p.Leu57= | |
ENST00000506357.5:c.155T= | ||
ENST00000514133.1:c.136T= | ENSP00000425818.1:p.Leu46= | |
NM_000232.4:c.169T= , LRG_204t1:c.169T= | NP_000223.1:p.Leu57= | |
XM_006714049.2:c.-239T= | XP_006714112.1:n.-239T= | |
XM_011534403.1:c.34-3642T= | XP_011532705.1:n.34-3642T= | |
XM_011534404.1:c.-216T= | XP_011532706.1:n.-216T= | |
NM_000232.5:c.169T= MANE Select | NP_000223.1:p.Leu57= |