HGVS | Genome Assembly |
---|---|
NC_000020.11:g.33438918C= , CM000682.2:g.33438918C= | GRCh38 |
NC_000020.10:g.32026724C= , CM000682.1:g.32026724C= | GRCh37 |
NC_000020.9:g.31490385C= | NCBI36 |
NG_011622.1:g.9975G= , LRG_332:g.9975G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000217381.3:c.419G= MANE Select | ENSP00000217381.2:p.Gly140= | |
ENST00000217381.2:c.419G= | ENSP00000217381.2:p.Gly140= | |
NM_003098.2:c.419G= , LRG_332t1:c.419G= | NP_003089.1:p.Gly140= | |
XM_005260517.1:c.419G= | XP_005260574.1:p.Gly140= | |
XM_011529007.1:c.419G= | XP_011527309.1:p.Gly140= | |
XM_011529008.1:c.419G= | XP_011527310.1:p.Gly140= | |
XR_936612.1:n.652G= | ||
XM_024451971.1:c.92G= | XP_024307739.1:p.Gly31= | |
NM_003098.3:c.419G= MANE Select | NP_003089.1:p.Gly140= |