HGVS | Genome Assembly |
---|---|
NC_000013.11:g.27920143A>C , CM000675.2:g.27920143A>C | GRCh38 |
NC_000013.10:g.28494280A>C , CM000675.1:g.28494280A>C | GRCh37 |
NC_000013.9:g.27392280A>C | NCBI36 |
NG_008183.1:g.5113A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381033.5:c.5A>C (PDX1) MANE Select | ENSP00000370421.4:p.Asn2Thr | |
ENST00000381033.4:c.5A>C (PDX1) | ENSP00000370421.4:p.Asn2Thr | |
NM_000209.3:c.5A>C (PDX1) | NP_000200.1:p.Asn2Thr | |
NR_047484.1:n.241+1021T>G (PLUT) | ||
XR_941578.1:n.150A>C (PDX1) | ||
XR_941579.1:n.150A>C (PDX1) | ||
XR_941580.1:n.150A>C (PDX1) | ||
XR_941578.2:n.162A>C (PDX1) | ||
XR_941580.2:n.162A>C (PDX1) | ||
NM_000209.4:c.5A>C (PDX1) MANE Select | NP_000200.1:p.Asn2Thr |