Canonical Allele Identifier: CA483027015
Gene: PDX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.28498814T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924677T>G , CM000675.2:g.27924677T>G GRCh38
NC_000013.10:g.28498814T>G , CM000675.1:g.28498814T>G GRCh37
NC_000013.9:g.27396814T>G NCBI36
NG_008183.1:g.9647T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.828T>G MANE Select ENSP00000370421.4:p.Pro276=
ENST00000381033.4:c.828T>G ENSP00000370421.4:p.Pro276=
NM_000209.3:c.828T>G NP_000200.1:p.Pro276=
NM_000209.4:c.828T>G MANE Select NP_000200.1:p.Pro276=
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Search 100 bp 3'