HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52028039C= , CM000666.2:g.52028039C= | GRCh38 |
NC_000004.11:g.52894205C= , CM000666.1:g.52894205C= | GRCh37 |
NC_000004.10:g.52588962C= | NCBI36 |
NG_008891.1:g.15281G= , LRG_204:g.15281G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.10:c.682G= MANE Select | ENSP00000370839.6:p.Gly228= | |
ENST00000381431.9:c.682G= | ENSP00000370839.5:p.Gly228= | |
NM_000232.4:c.682G= , LRG_204t1:c.682G= | NP_000223.1:p.Gly228= | |
XM_006714049.2:c.385G= | XP_006714112.1:p.Gly129= | |
XM_011534403.1:c.472G= | XP_011532705.1:p.Gly158= | |
XM_011534404.1:c.385G= | XP_011532706.1:p.Gly129= | |
NM_000232.5:c.682G= MANE Select | NP_000223.1:p.Gly228= |