HGVS | Genome Assembly |
---|---|
NC_000017.11:g.70175661C= , CM000679.2:g.70175661C= | GRCh38 |
NC_000017.10:g.68171802C= , CM000679.1:g.68171802C= | GRCh37 |
NC_000017.9:g.65683397C= | NCBI36 |
NG_008798.1:g.11127C= , LRG_328:g.11127C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000243457.4:c.622C= MANE Select | ENSP00000243457.2:p.Leu208= | |
ENST00000243457.3:c.622C= | ENSP00000243457.2:p.Leu208= | |
ENST00000535240.1:c.622C= | ENSP00000441848.1:p.Leu208= | |
NM_000891.2:c.622C= , LRG_328t1:c.622C= | NP_000882.1:p.Leu208= | |
XM_011524779.1:c.622C= | XP_011523081.1:p.Leu208= | |
NM_000891.3:c.622C= MANE Select | NP_000882.1:p.Leu208= |