HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17401329C>T , CM000663.2:g.17401329C>T | GRCh38 |
NC_000001.10:g.17727825C>T , CM000663.1:g.17727825C>T | GRCh37 |
NC_000001.9:g.17600412C>T | NCBI36 |
NG_032943.1:g.34084C>T | |
NG_032943.2:g.34084C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000619609.1:c.1976C>T MANE Select | ENSP00000483125.1:p.Thr659Ile | |
NM_207421.4:c.1976C>T MANE Select | NP_997304.3:p.Thr659Ile |