Canonical Allele Identifier: CA483175599

Linked Data

dbSNP Id: rs925409013
MyVariant Identifiers: chr13:g.28494374T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27920237T>G , CM000675.2:g.27920237T>G GRCh38
NC_000013.10:g.28494374T>G , CM000675.1:g.28494374T>G GRCh37
NC_000013.9:g.27392374T>G NCBI36
NG_008183.1:g.5207T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.99T>G (PDX1) MANE Select ENSP00000370421.4:p.Pro33=
ENST00000381033.4:c.99T>G (PDX1) ENSP00000370421.4:p.Pro33=
NM_000209.3:c.99T>G (PDX1) NP_000200.1:p.Pro33=
NR_047484.1:n.241+927A>C (PLUT)
XR_941578.1:n.244T>G (PDX1)
XR_941579.1:n.244T>G (PDX1)
XR_941580.1:n.244T>G (PDX1)
XR_941578.2:n.256T>G (PDX1)
XR_941580.2:n.256T>G (PDX1)
NM_000209.4:c.99T>G (PDX1) MANE Select NP_000200.1:p.Pro33=