Canonical Allele Identifier: CA2080721304
Gene: PDX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924508T= , CM000675.2:g.27924508T= GRCh38
NC_000013.10:g.28498645T= , CM000675.1:g.28498645T= GRCh37
NC_000013.9:g.27396645T= NCBI36
NG_008183.1:g.9478T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.659T= MANE Select ENSP00000370421.4:p.Val220=
ENST00000381033.4:c.659T= ENSP00000370421.4:p.Val220=
NM_000209.3:c.659T= NP_000200.1:p.Val220=
NM_000209.4:c.659T= MANE Select NP_000200.1:p.Val220=
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Search 100 bp 3'