HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52028021T= , CM000666.2:g.52028021T= | GRCh38 |
NC_000004.11:g.52894187T= , CM000666.1:g.52894187T= | GRCh37 |
NC_000004.10:g.52588944T= | NCBI36 |
NG_008891.1:g.15299A= , LRG_204:g.15299A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.10:c.700A= MANE Select | ENSP00000370839.6:p.Ile234= | |
ENST00000381431.9:c.700A= | ENSP00000370839.5:p.Ile234= | |
NM_000232.4:c.700A= , LRG_204t1:c.700A= | NP_000223.1:p.Ile234= | |
XM_006714049.2:c.403A= | XP_006714112.1:p.Ile135= | |
XM_011534403.1:c.490A= | XP_011532705.1:p.Ile164= | |
XM_011534404.1:c.403A= | XP_011532706.1:p.Ile135= | |
NM_000232.5:c.700A= MANE Select | NP_000223.1:p.Ile234= |