HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19954334T= , CM000670.2:g.19954334T= | GRCh38 |
NC_000008.10:g.19811845T= , CM000670.1:g.19811845T= | GRCh37 |
NC_000008.9:g.19856125T= | NCBI36 |
NG_008855.1:g.20264T= | |
NG_008855.2:g.57618T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650287.1:c.756T= MANE Select | ENSP00000497642.1:p.Ile252= | |
ENST00000311322.8:c.756T= | ENSP00000309757.6:p.Ile252= | |
NM_000237.2:c.756T= | NP_000228.1:p.Ile252= | |
NM_000237.3:c.756T= MANE Select | NP_000228.1:p.Ile252= |