HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32220590T>A , CM000668.2:g.32220590T>A | GRCh38 |
NC_000006.11:g.32188367T>A , CM000668.1:g.32188367T>A | GRCh37 |
NC_000006.10:g.32296345T>A | NCBI36 |
NG_028190.1:g.8478A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375023.3:c.974A>T MANE Select | ENSP00000364163.3:p.His325Leu | |
ENST00000473562.1:n.1103A>T | ||
NM_004557.3:c.974A>T | NP_004548.3:p.His325Leu | |
NR_134949.1:n.1113A>T | ||
NR_134950.1:n.1113A>T | ||
NM_004557.4:c.974A>T MANE Select | NP_004548.3:p.His325Leu | |
NR_134949.2:n.1113A>T | ||
NR_134950.2:n.1113A>T |