HGVS | Genome Assembly |
---|---|
NC_000002.12:g.70831778A>T , CM000664.2:g.70831778A>T | GRCh38 |
NC_000002.11:g.71058909A>T , CM000664.1:g.71058909A>T | GRCh37 |
NC_000002.10:g.70912417A>T | NCBI36 |
NG_033914.1:g.9046T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000410009.5:c.759T>A MANE Select | ENSP00000386378.3:p.Ile253= | |
ENST00000410009.4:c.759T>A | ENSP00000386378.3:p.Ile253= | |
NM_015717.4:c.759T>A | NP_056532.4:p.Ile253= | |
XM_011532874.1:c.759T>A | XP_011531176.1:p.Ile253= | |
XM_011532875.1:c.759T>A | XP_011531177.1:p.Ile253= | |
XM_011532876.1:c.759T>A | XP_011531178.1:p.Ile253= | |
XM_011532875.2:c.759T>A | XP_011531177.1:p.Ile253= | |
XM_011532876.2:c.759T>A | XP_011531178.1:p.Ile253= | |
NM_015717.5:c.759T>A MANE Select | NP_056532.4:p.Ile253= |