HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17022645C= , CM000663.2:g.17022645C= | GRCh38 |
NC_000001.10:g.17349140C= , CM000663.1:g.17349140C= | GRCh37 |
NC_000001.9:g.17221727C= | NCBI36 |
NG_012340.1:g.36526G= , LRG_316:g.36526G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000463045.3:c.557G= | ENSP00000481376.2:p.Cys186= | |
ENST00000491274.6:c.686G= | ENSP00000480482.2:p.Cys229= | |
ENST00000375499.8:c.728G= MANE Select | ENSP00000364649.3:p.Cys243= | |
ENST00000375499.7:c.728G= | ENSP00000364649.3:p.Cys243= | |
ENST00000475049.5:n.153G= | ||
ENST00000485092.5:n.392G= | ||
ENST00000485515.5:n.662G= | ||
NM_003000.2:c.728G= , LRG_316t1:c.728G= | NP_002991.2:p.Cys243= | |
NM_003000.3:c.728G= MANE Select | NP_002991.2:p.Cys243= |