Canonical Allele Identifier: CA387645452
Gene: PDX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.28498485T>A (hg19) chr13:g.27924348T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924348T>A , CM000675.2:g.27924348T>A GRCh38
NC_000013.10:g.28498485T>A , CM000675.1:g.28498485T>A GRCh37
NC_000013.9:g.27396485T>A NCBI36
NG_008183.1:g.9318T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.499T>A MANE Select ENSP00000370421.4:p.Phe167Ile
ENST00000381033.4:c.499T>A ENSP00000370421.4:p.Phe167Ile
NM_000209.3:c.499T>A NP_000200.1:p.Phe167Ile
NM_000209.4:c.499T>A MANE Select NP_000200.1:p.Phe167Ile
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