HGVS | Genome Assembly |
---|---|
NC_000017.11:g.29495560C>T , CM000679.2:g.29495560C>T | GRCh38 |
NC_000017.10:g.27822578C>T , CM000679.1:g.27822578C>T | GRCh37 |
NC_000017.9:g.24846704C>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261716.8:c.832C>T MANE Select | ENSP00000261716.3:p.His278Tyr | |
ENST00000261716.7:c.832C>T | ENSP00000261716.3:p.His278Tyr | |
ENST00000536202.1:c.832C>T | ENSP00000438819.1:p.His278Tyr | |
ENST00000577583.1:n.680C>T | ||
NM_020791.2:c.832C>T | NP_065842.1:p.His278Tyr | |
NM_025142.1:c.832C>T | NP_079418.1:p.His278Tyr | |
XM_011525060.1:c.832C>T | XP_011523362.1:p.His278Tyr | |
XM_011525060.2:c.832C>T | XP_011523362.1:p.His278Tyr | |
NM_020791.4:c.832C>T MANE Select | NP_065842.1:p.His278Tyr |