HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154997095C= , CM000685.2:g.154997095C= | GRCh38 |
NC_000023.10:g.154225370C= , CM000685.1:g.154225370C= | GRCh37 |
NC_000023.9:g.153878564C= | NCBI36 |
NG_011403.1:g.30629G= | |
NG_011403.2:g.30629G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000360256.9:c.266G= MANE Select | ENSP00000353393.4:p.Gly89= | |
ENST00000647125.1:c.*52G= | ENSP00000496062.1:n.*52G= | |
ENST00000360256.8:c.266G= | ENSP00000353393.4:p.Gly89= | |
ENST00000423959.5:c.161G= | ENSP00000409446.1:p.Gly54= | |
ENST00000453950.1:c.248G= | ENSP00000389153.1:p.Gly83= | |
NM_000132.3:c.266G= | NP_000123.1:p.Gly89= | |
XM_011531126.1:c.161G= | XP_011529428.1:p.Gly54= | |
NM_000132.4:c.266G= MANE Select | NP_000123.1:p.Gly89= |