HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52033448C= , CM000666.2:g.52033448C= | GRCh38 |
NC_000004.11:g.52899614C= , CM000666.1:g.52899614C= | GRCh37 |
NC_000004.10:g.52594371C= | NCBI36 |
NG_008891.1:g.9872G= , LRG_204:g.9872G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.10:c.226G= MANE Select | ENSP00000370839.6:p.Ala76= | |
ENST00000381431.9:c.226G= | ENSP00000370839.5:p.Ala76= | |
ENST00000506357.5:c.212G= | ||
ENST00000514133.1:c.193G= | ENSP00000425818.1:p.Ala65= | |
NM_000232.4:c.226G= , LRG_204t1:c.226G= | NP_000223.1:p.Ala76= | |
XM_006714049.2:c.-182G= | XP_006714112.1:n.-182G= | |
XM_011534403.1:c.34-3585G= | XP_011532705.1:n.34-3585G= | |
XM_011534404.1:c.-159G= | XP_011532706.1:n.-159G= | |
NM_000232.5:c.226G= MANE Select | NP_000223.1:p.Ala76= |