HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52028084T= , CM000666.2:g.52028084T= | GRCh38 |
NC_000004.11:g.52894250T= , CM000666.1:g.52894250T= | GRCh37 |
NC_000004.10:g.52589007T= | NCBI36 |
NG_008891.1:g.15236A= , LRG_204:g.15236A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.10:c.637A= MANE Select | ENSP00000370839.6:p.Thr213= | |
ENST00000381431.9:c.637A= | ENSP00000370839.5:p.Thr213= | |
NM_000232.4:c.637A= , LRG_204t1:c.637A= | NP_000223.1:p.Thr213= | |
XM_006714049.2:c.340A= | XP_006714112.1:p.Thr114= | |
XM_011534403.1:c.427A= | XP_011532705.1:p.Thr143= | |
XM_011534404.1:c.340A= | XP_011532706.1:p.Thr114= | |
NM_000232.5:c.637A= MANE Select | NP_000223.1:p.Thr213= |