HGVS | Genome Assembly |
---|---|
NC_000017.11:g.16948754G>T , CM000679.2:g.16948754G>T | GRCh38 |
NC_000017.10:g.16852068G>T , CM000679.1:g.16852068G>T | GRCh37 |
NC_000017.9:g.16792793G>T | NCBI36 |
NG_007281.1:g.28335C>A , LRG_120:g.28335C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261652.7:c.429C>A MANE Select | ENSP00000261652.2:p.Gly143= | |
ENST00000261652.6:c.429C>A | ENSP00000261652.2:p.Gly143= | |
ENST00000579315.5:c.429C>A | ENSP00000464069.1:p.Gly143= | |
ENST00000581616.2:n.432C>A | ||
ENST00000582931.5:n.333C>A | ||
ENST00000583789.1:c.291C>A | ENSP00000462952.1:p.Gly97= | |
ENST00000584950.5:c.291C>A | ENSP00000463582.1:p.Gly97= | |
NM_012452.2:c.429C>A , LRG_120t1:c.429C>A | NP_036584.1:p.Gly143= | |
NM_012452.3:c.429C>A MANE Select | NP_036584.1:p.Gly143= |