Canonical Allele Identifier: CA2622478655
Gene: PDX1 HGNC NCBI

Linked Data

gnomAD v4: 13-27924842-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924842G>A , CM000675.2:g.27924842G>A GRCh38
NC_000013.10:g.28498979G>A , CM000675.1:g.28498979G>A GRCh37
NC_000013.9:g.27396979G>A NCBI36
NG_008183.1:g.9812G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*141G>A MANE Select ENSP00000370421.4:n.*141G>A
ENST00000381033.4:c.*141G>A ENSP00000370421.4:n.*141G>A
NM_000209.3:c.*141G>A NP_000200.1:n.*141G>A
NM_000209.4:c.*141G>A MANE Select NP_000200.1:n.*141G>A
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