HGVS | Genome Assembly |
---|---|
NC_000013.11:g.110166198A= , CM000675.2:g.110166198A= | GRCh38 |
NC_000013.10:g.110818545A= , CM000675.1:g.110818545A= | GRCh37 |
NC_000013.9:g.109616546A= | NCBI36 |
NG_011544.2:g.145952T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000375820.10:c.4021+34T= MANE Select | ENSP00000364979.4:n.4021+34T= | |
ENST00000650424.1:c.177+34T= | ||
ENST00000375820.8:c.4021+34T= | ENSP00000364979.4:n.4021+34T= | |
NM_001845.5:c.4021+34T= | NP_001836.3:n.4021+34T= | |
XM_011521048.1:c.3829+34T= | XP_011519350.1:n.3829+34T= | |
XM_011521048.2:c.3829+34T= | XP_011519350.1:n.3829+34T= | |
NM_001845.6:c.4021+34T= MANE Select | NP_001836.3:n.4021+34T= |