HGVS | Genome Assembly |
---|---|
NC_000001.11:g.84399513C>T , CM000663.2:g.84399513C>T | GRCh38 |
NC_000001.10:g.84865196C>T , CM000663.1:g.84865196C>T | GRCh37 |
NC_000001.9:g.84637784C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370665.4:c.125+824C>T MANE Select | ENSP00000359699.3:n.125+824C>T | |
ENST00000370665.3:c.125+824C>T | ENSP00000359699.3:n.125+824C>T | |
NM_021233.2:c.125+824C>T | NP_067056.2:n.125+824C>T | |
NM_021233.3:c.125+824C>T MANE Select | NP_067056.2:n.125+824C>T |