HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169555334A= , CM000663.2:g.169555334A= | GRCh38 |
NC_000001.10:g.169524572A= , CM000663.1:g.169524572A= | GRCh37 |
NC_000001.9:g.167791196A= | NCBI36 |
NG_011806.1:g.36198T= , LRG_553:g.36198T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367797.9:c.966T= MANE Select | ENSP00000356771.3:p.Ala322= | |
ENST00000367796.3:c.966T= | ENSP00000356770.3:p.Ala322= | |
ENST00000367797.7:c.966T= | ENSP00000356771.3:p.Ala322= | |
NM_000130.4:c.966T= , LRG_553t1:c.966T= | NP_000121.2:p.Ala322= | |
XM_017000660.2:c.555T= | XP_016856149.1:p.Ala185= | |
NM_000130.5:c.966T= MANE Select | NP_000121.2:p.Ala322= |