HGVS | Genome Assembly |
---|---|
NC_000016.10:g.67436258C>T , CM000678.2:g.67436258C>T | GRCh38 |
NC_000016.9:g.67470161C>T , CM000678.1:g.67470161C>T | GRCh37 |
NC_000016.8:g.66027662C>T | NCBI36 |
NG_011482.1:g.49929G>A | |
NG_016549.1:g.10126C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000326152.6:c.674C>T MANE Select | ENSP00000316786.5:p.Pro225Leu | |
ENST00000326152.5:c.674C>T | ENSP00000316786.5:p.Pro225Leu | |
ENST00000567684.2:n.537C>T | ||
NM_000196.3:c.674C>T | NP_000187.3:p.Pro225Leu | |
NM_000196.4:c.674C>T MANE Select | NP_000187.3:p.Pro225Leu |