HGVS | Genome Assembly |
---|---|
NC_000012.12:g.110911097G>A , CM000674.2:g.110911097G>A | GRCh38 |
NC_000012.11:g.111348901G>A , CM000674.1:g.111348901G>A | GRCh37 |
NC_000012.10:g.109833284G>A | NCBI36 |
NG_007554.1:g.14481C>T , LRG_393:g.14481C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000228841.15:c.481C>T MANE Select | ENSP00000228841.8:p.His161Tyr | |
ENST00000663220.1:c.424C>T | ENSP00000499568.1:p.His142Tyr | |
ENST00000228841.12:c.481C>T | ENSP00000228841.7:p.His161Tyr | |
ENST00000548438.1:c.439C>T | ENSP00000447154.1:p.His147Tyr | |
NM_000432.3:c.481C>T , LRG_393t1:c.481C>T | NP_000423.2:p.His161Tyr | |
NM_000432.4:c.481C>T MANE Select | NP_000423.2:p.His161Tyr |