HGVS | Genome Assembly |
---|---|
NC_000013.11:g.27920195G>A , CM000675.2:g.27920195G>A | GRCh38 |
NC_000013.10:g.28494332G>A , CM000675.1:g.28494332G>A | GRCh37 |
NC_000013.9:g.27392332G>A | NCBI36 |
NG_008183.1:g.5165G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381033.5:c.57G>A (PDX1) MANE Select | ENSP00000370421.4:p.Ala19= | |
ENST00000381033.4:c.57G>A (PDX1) | ENSP00000370421.4:p.Ala19= | |
NM_000209.3:c.57G>A (PDX1) | NP_000200.1:p.Ala19= | |
NR_047484.1:n.241+969C>T (PLUT) | ||
XR_941578.1:n.202G>A (PDX1) | ||
XR_941579.1:n.202G>A (PDX1) | ||
XR_941580.1:n.202G>A (PDX1) | ||
XR_941578.2:n.214G>A (PDX1) | ||
XR_941580.2:n.214G>A (PDX1) | ||
NM_000209.4:c.57G>A (PDX1) MANE Select | NP_000200.1:p.Ala19= |