HGVS | Genome Assembly |
---|---|
NC_000017.11:g.16948889C>T , CM000679.2:g.16948889C>T | GRCh38 |
NC_000017.10:g.16852203C>T , CM000679.1:g.16852203C>T | GRCh37 |
NC_000017.9:g.16792928C>T | NCBI36 |
NG_007281.1:g.28200G>A , LRG_120:g.28200G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261652.7:c.294G>A MANE Select | ENSP00000261652.2:p.Lys98= | |
ENST00000261652.6:c.294G>A | ENSP00000261652.2:p.Lys98= | |
ENST00000579315.5:c.294G>A | ENSP00000464069.1:p.Lys98= | |
ENST00000581616.2:n.297G>A | ||
ENST00000582931.5:n.198G>A | ||
ENST00000583789.1:c.156G>A | ENSP00000462952.1:p.Lys52= | |
ENST00000584950.5:c.156G>A | ENSP00000463582.1:p.Lys52= | |
NM_012452.2:c.294G>A , LRG_120t1:c.294G>A | NP_036584.1:p.Lys98= | |
NM_012452.3:c.294G>A MANE Select | NP_036584.1:p.Lys98= |