Canonical Allele Identifier: CA2622478473
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs2137506762
gnomAD v4: 13-27924757-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924757A>G , CM000675.2:g.27924757A>G GRCh38
NC_000013.10:g.28498894A>G , CM000675.1:g.28498894A>G GRCh37
NC_000013.9:g.27396894A>G NCBI36
NG_008183.1:g.9727A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*56A>G MANE Select ENSP00000370421.4:n.*56A>G
ENST00000381033.4:c.*56A>G ENSP00000370421.4:n.*56A>G
NM_000209.3:c.*56A>G NP_000200.1:n.*56A>G
NM_000209.4:c.*56A>G MANE Select NP_000200.1:n.*56A>G
Search 100 bp 5'
Search 100 bp 3'