HGVS | Genome Assembly |
---|---|
NC_000022.11:g.26607864C= , CM000684.2:g.26607864C= | GRCh38 |
NC_000022.10:g.27003828C= , CM000684.1:g.27003828C= | GRCh37 |
NC_000022.9:g.25333828C= | NCBI36 |
NG_009826.1:g.15164G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647569.1:n.244+25G= | ||
ENST00000647684.1:c.432+25G= MANE Select | ENSP00000497249.1:n.432+25G= | |
ENST00000215939.2:c.432+25G= | ENSP00000215939.2:n.432+25G= | |
NM_001887.3:c.432+25G= | NP_001878.1:n.432+25G= | |
XM_011529899.1:c.432+25G= | XP_011528201.1:n.432+25G= | |
NM_001887.4:c.432+25G= MANE Select | NP_001878.1:n.432+25G= | |
XM_011529899.3:c.432+25G= | XP_011528201.1:n.432+25G= |