HGVS | Genome Assembly |
---|---|
NC_000001.11:g.115738274A>G , CM000663.2:g.115738274A>G | GRCh38 |
NC_000001.10:g.116280895A>G , CM000663.1:g.116280895A>G | GRCh37 |
NC_000001.9:g.116082418A>G | NCBI36 |
NG_008802.1:g.35532T>C , LRG_404:g.35532T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000488931.2:c.206T>C | ENSP00000518226.1:p.Ile69Thr | |
ENST00000261448.6:c.482T>C MANE Select | ENSP00000261448.5:p.Ile161Thr | |
ENST00000261448.5:c.482T>C | ENSP00000261448.5:p.Ile161Thr | |
NM_001232.3:c.482T>C , LRG_404t1:c.482T>C | NP_001223.2:p.Ile161Thr | |
NM_001232.4:c.482T>C MANE Select | NP_001223.2:p.Ile161Thr |