HGVS | Genome Assembly |
---|---|
NC_000002.12:g.47377045C>T , CM000664.2:g.47377045C>T | GRCh38 |
NC_000002.11:g.47604184C>T , CM000664.1:g.47604184C>T | GRCh37 |
NC_000002.10:g.47457688C>T | NCBI36 |
NG_012352.2:g.36883C>T , LRG_215:g.36883C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263735.9:c.523C>T MANE Select | ENSP00000263735.4:p.Gln175Ter | |
ENST00000263735.8:c.523C>T | ENSP00000263735.4:p.Gln175Ter | |
ENST00000405271.5:c.607C>T | ENSP00000385476.1:p.Gln203Ter | |
ENST00000456133.5:c.607C>T | ENSP00000410675.1:p.Gln203Ter | |
ENST00000490733.1:n.372C>T | ||
NM_002354.2:c.523C>T , LRG_215t1:c.523C>T | NP_002345.2:p.Gln175Ter | |
NM_002354.3:c.523C>T MANE Select | NP_002345.2:p.Gln175Ter |