Canonical Allele Identifier: CA2622478496
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924767A>G , CM000675.2:g.27924767A>G GRCh38
NC_000013.10:g.28498904A>G , CM000675.1:g.28498904A>G GRCh37
NC_000013.9:g.27396904A>G NCBI36
NG_008183.1:g.9737A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*66A>G MANE Select ENSP00000370421.4:n.*66A>G
ENST00000381033.4:c.*66A>G ENSP00000370421.4:n.*66A>G
NM_000209.3:c.*66A>G NP_000200.1:n.*66A>G
NM_000209.4:c.*66A>G MANE Select NP_000200.1:n.*66A>G