Canonical Allele Identifier: CA387645339
Gene: PDX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.28498434C>G (hg19) chr13:g.27924297C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924297C>G , CM000675.2:g.27924297C>G GRCh38
NC_000013.10:g.28498434C>G , CM000675.1:g.28498434C>G GRCh37
NC_000013.9:g.27396434C>G NCBI36
NG_008183.1:g.9267C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.448C>G MANE Select ENSP00000370421.4:p.Arg150Gly
ENST00000381033.4:c.448C>G ENSP00000370421.4:p.Arg150Gly
NM_000209.3:c.448C>G NP_000200.1:p.Arg150Gly
XR_941578.1:n.3575C>G
XR_941579.1:n.2174C>G
XR_941580.1:n.1090C>G
XR_941578.2:n.3587C>G
XR_941580.2:n.1102C>G
NM_000209.4:c.448C>G MANE Select NP_000200.1:p.Arg150Gly
Search 100 bp 5'
Search 100 bp 3'