HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87727464C>T , CM000672.2:g.87727464C>T | GRCh38 |
NC_000010.10:g.89487221C>T , CM000672.1:g.89487221C>T | GRCh37 |
NC_000010.9:g.89477201C>T | NCBI36 |
NG_012150.1:g.72746C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000456849.2:c.1061C>T MANE Select | ENSP00000406157.1:p.Thr354Ile | |
ENST00000361175.8:c.1046C>T | ENSP00000354436.4:p.Thr349Ile | |
ENST00000456849.1:c.1061C>T | ENSP00000406157.1:p.Thr354Ile | |
NM_001015880.1:c.1061C>T | NP_001015880.1:p.Thr354Ile | |
NM_004670.3:c.1046C>T | NP_004661.2:p.Thr349Ile | |
NM_001015880.2:c.1061C>T MANE Select | NP_001015880.1:p.Thr354Ile | |
NM_004670.4:c.1046C>T | NP_004661.2:p.Thr349Ile |