HGVS | Genome Assembly |
---|---|
NC_000002.12:g.47377046A= , CM000664.2:g.47377046A= | GRCh38 |
NC_000002.11:g.47604185A= , CM000664.1:g.47604185A= | GRCh37 |
NC_000002.10:g.47457689A= | NCBI36 |
NG_012352.2:g.36884A= , LRG_215:g.36884A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263735.9:c.524A= MANE Select | ENSP00000263735.4:p.Gln175= | |
ENST00000263735.8:c.524A= | ENSP00000263735.4:p.Gln175= | |
ENST00000405271.5:c.608A= | ENSP00000385476.1:p.Gln203= | |
ENST00000456133.5:c.608A= | ENSP00000410675.1:p.Gln203= | |
ENST00000490733.1:n.373A= | ||
NM_002354.2:c.524A= , LRG_215t1:c.524A= | NP_002345.2:p.Gln175= | |
NM_002354.3:c.524A= MANE Select | NP_002345.2:p.Gln175= |