HGVS | Genome Assembly |
---|---|
NC_000017.11:g.70175617T= , CM000679.2:g.70175617T= | GRCh38 |
NC_000017.10:g.68171758T= , CM000679.1:g.68171758T= | GRCh37 |
NC_000017.9:g.65683353T= | NCBI36 |
NG_008798.1:g.11083T= , LRG_328:g.11083T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000243457.4:c.578T= MANE Select | ENSP00000243457.2:p.Leu193= | |
ENST00000243457.3:c.578T= | ENSP00000243457.2:p.Leu193= | |
ENST00000535240.1:c.578T= | ENSP00000441848.1:p.Leu193= | |
NM_000891.2:c.578T= , LRG_328t1:c.578T= | NP_000882.1:p.Leu193= | |
XM_011524779.1:c.578T= | XP_011523081.1:p.Leu193= | |
NM_000891.3:c.578T= MANE Select | NP_000882.1:p.Leu193= |