Canonical Allele Identifier: CA2080721483
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1957814038
gnomAD v4: 13-27924828-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924828C>T , CM000675.2:g.27924828C>T GRCh38
NC_000013.10:g.28498965C>T , CM000675.1:g.28498965C>T GRCh37
NC_000013.9:g.27396965C>T NCBI36
NG_008183.1:g.9798C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*127C>T MANE Select ENSP00000370421.4:n.*127C>T
ENST00000381033.4:c.*127C>T ENSP00000370421.4:n.*127C>T
NM_000209.3:c.*127C>T NP_000200.1:n.*127C>T
NM_000209.4:c.*127C>T MANE Select NP_000200.1:n.*127C>T
Search 100 bp 5'
Search 100 bp 3'