Canonical Allele Identifier: CA387643826

Linked Data

dbSNP Id: rs2137502271

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27920229A>G , CM000675.2:g.27920229A>G GRCh38
NC_000013.10:g.28494366A>G , CM000675.1:g.28494366A>G GRCh37
NC_000013.9:g.27392366A>G NCBI36
NG_008183.1:g.5199A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.91A>G (PDX1) MANE Select ENSP00000370421.4:p.Ser31Gly
ENST00000381033.4:c.91A>G (PDX1) ENSP00000370421.4:p.Ser31Gly
NM_000209.3:c.91A>G (PDX1) NP_000200.1:p.Ser31Gly
NR_047484.1:n.241+935T>C (PLUT)
XR_941578.1:n.236A>G (PDX1)
XR_941579.1:n.236A>G (PDX1)
XR_941580.1:n.236A>G (PDX1)
XR_941578.2:n.248A>G (PDX1)
XR_941580.2:n.248A>G (PDX1)
NM_000209.4:c.91A>G (PDX1) MANE Select NP_000200.1:p.Ser31Gly