HGVS | Genome Assembly |
---|---|
NC_000021.9:g.44290047C= , CM000683.2:g.44290047C= | GRCh38 |
NC_000021.8:g.45709930C= , CM000683.1:g.45709930C= | GRCh37 |
NC_000021.7:g.44534358C= | NCBI36 |
NG_009556.1:g.9168C= , LRG_18:g.9168C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291582.6:c.858C= MANE Select | ENSP00000291582.5:p.Pro286= | |
ENST00000291582.5:c.858C= | ENSP00000291582.5:p.Pro286= | |
ENST00000527919.5:n.1591C= | ||
ENST00000530812.5:n.2608C= | ||
NM_000383.3:c.858C= | NP_000374.1:p.Pro286= | |
XM_011529551.1:c.858C= | XP_011527853.1:p.Pro286= | |
NM_000383.4:c.858C= MANE Select | NP_000374.1:p.Pro286= |