HGVS | Genome Assembly |
---|---|
NC_000002.12:g.70831715C>T , CM000664.2:g.70831715C>T | GRCh38 |
NC_000002.11:g.71058846C>T , CM000664.1:g.71058846C>T | GRCh37 |
NC_000002.10:g.70912354C>T | NCBI36 |
NG_033914.1:g.9109G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000410009.5:c.822G>A MANE Select | ENSP00000386378.3:p.Lys274= | |
ENST00000410009.4:c.822G>A | ENSP00000386378.3:p.Lys274= | |
NM_015717.4:c.822G>A | NP_056532.4:p.Lys274= | |
XM_011532874.1:c.822G>A | XP_011531176.1:p.Lys274= | |
XM_011532875.1:c.822G>A | XP_011531177.1:p.Lys274= | |
XM_011532876.1:c.822G>A | XP_011531178.1:p.Lys274= | |
XM_011532875.2:c.822G>A | XP_011531177.1:p.Lys274= | |
XM_011532876.2:c.822G>A | XP_011531178.1:p.Lys274= | |
NM_015717.5:c.822G>A MANE Select | NP_056532.4:p.Lys274= |