HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55063532C>A , CM000663.2:g.55063532C>A | GRCh38 |
NC_000001.10:g.55529205C>A , CM000663.1:g.55529205C>A | GRCh37 |
NC_000001.9:g.55301793C>A | NCBI36 |
NG_009061.1:g.28986C>A , LRG_275:g.28986C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673913.2:c.*367C>A | ENSP00000501161.2:n.*367C>A | |
ENST00000710286.1:c.2384C>A | ENSP00000518176.1:p.Ala795Asp | |
ENST00000673903.1:c.1652C>A | ENSP00000501257.1:p.Ala551Asp | |
ENST00000302118.5:c.2027C>A MANE Select | ENSP00000303208.5:p.Ala676Asp | |
ENST00000490692.1:n.2573C>A | ||
NM_174936.3:c.2027C>A , LRG_275t1:c.2027C>A | NP_777596.2:p.Ala676Asp | |
NR_110451.1:n.1634C>A | ||
XM_011541193.1:c.1148C>A | XP_011539495.1:p.Ala383Asp | |
NM_174936.4:c.2027C>A MANE Select | NP_777596.2:p.Ala676Asp | |
NR_110451.2:n.1634C>A |