HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17381972A= , CM000663.2:g.17381972A= | GRCh38 |
NC_000001.10:g.17708467A= , CM000663.1:g.17708467A= | GRCh37 |
NC_000001.9:g.17581054A= | NCBI36 |
NG_032943.1:g.14727A= | |
NG_032943.2:g.14727A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000619609.1:c.559A= MANE Select | ENSP00000483125.1:p.Thr187= | |
NM_207421.4:c.559A= MANE Select | NP_997304.3:p.Thr187= |