HGVS | Genome Assembly |
---|---|
NC_000017.11:g.70175841A= , CM000679.2:g.70175841A= | GRCh38 |
NC_000017.10:g.68171982A= , CM000679.1:g.68171982A= | GRCh37 |
NC_000017.9:g.65683577A= | NCBI36 |
NG_008798.1:g.11307A= , LRG_328:g.11307A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000243457.4:c.802A= MANE Select | ENSP00000243457.2:p.Thr268= | |
ENST00000243457.3:c.802A= | ENSP00000243457.2:p.Thr268= | |
ENST00000535240.1:c.802A= | ENSP00000441848.1:p.Thr268= | |
NM_000891.2:c.802A= , LRG_328t1:c.802A= | NP_000882.1:p.Thr268= | |
XM_011524779.1:c.802A= | XP_011523081.1:p.Thr268= | |
NM_000891.3:c.802A= MANE Select | NP_000882.1:p.Thr268= |