HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169541814G>T , CM000663.2:g.169541814G>T | GRCh38 |
NC_000001.10:g.169511052G>T , CM000663.1:g.169511052G>T | GRCh37 |
NC_000001.9:g.167777676G>T | NCBI36 |
NG_011806.1:g.49718C>A , LRG_553:g.49718C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000367797.9:c.3276C>A MANE Select | ENSP00000356771.3:p.Gly1092= | |
ENST00000367796.3:c.3291C>A | ENSP00000356770.3:p.Gly1097= | |
ENST00000367797.7:c.3276C>A | ENSP00000356771.3:p.Gly1092= | |
NM_000130.4:c.3276C>A , LRG_553t1:c.3276C>A | NP_000121.2:p.Gly1092= | |
XM_017000660.2:c.2865C>A | XP_016856149.1:p.Gly955= | |
NM_000130.5:c.3276C>A MANE Select | NP_000121.2:p.Gly1092= |