HGVS | Genome Assembly |
---|---|
NC_000009.12:g.6595069A= , CM000671.2:g.6595069A= | GRCh38 |
NC_000009.11:g.6595069A= , CM000671.1:g.6595069A= | GRCh37 |
NC_000009.10:g.6585069A= | NCBI36 |
NG_016397.1:g.55624T= , LRG_643:g.55624T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000321612.8:c.1206T= MANE Select | ENSP00000370737.4:p.His402= | |
ENST00000638654.1:c.453T= | ENSP00000491101.1:p.His151= | |
ENST00000639364.1:n.906T= | ||
ENST00000639443.1:n.774T= | ||
ENST00000639493.1:n.358T= | ||
ENST00000639954.1:n.914T= | ||
ENST00000640592.1:n.1089T= | ||
ENST00000321612.6:c.1206T= | ENSP00000370737.3:p.His402= | |
ENST00000463305.1:n.290T= | ||
NM_000170.2:c.1206T= , LRG_643t1:c.1206T= | NP_000161.2:p.His402= | |
NM_000170.3:c.1206T= MANE Select | NP_000161.2:p.His402= |