HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55043868A>C , CM000663.2:g.55043868A>C | GRCh38 |
NC_000001.10:g.55509541A>C , CM000663.1:g.55509541A>C | GRCh37 |
NC_000001.9:g.55282129A>C | NCBI36 |
NG_009061.1:g.9322A>C , LRG_275:g.9322A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000673913.2:c.233A>C | ENSP00000501161.2:p.Tyr78Ser | |
ENST00000710286.1:c.590A>C | ENSP00000518176.1:p.Tyr197Ser | |
ENST00000673726.1:c.233A>C | ENSP00000501004.1:p.Tyr78Ser | |
ENST00000673903.1:c.-143A>C | ENSP00000501257.1:n.-143A>C | |
ENST00000302118.5:c.233A>C MANE Select | ENSP00000303208.5:p.Tyr78Ser | |
NM_174936.3:c.233A>C , LRG_275t1:c.233A>C | NP_777596.2:p.Tyr78Ser | |
NR_110451.1:n.182+3465A>C | ||
NM_174936.4:c.233A>C MANE Select | NP_777596.2:p.Tyr78Ser | |
NR_110451.2:n.182+3465A>C |