Canonical Allele Identifier: CA608741262
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1275417800

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924727G>A , CM000675.2:g.27924727G>A GRCh38
NC_000013.10:g.28498864G>A , CM000675.1:g.28498864G>A GRCh37
NC_000013.9:g.27396864G>A NCBI36
NG_008183.1:g.9697G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*26G>A MANE Select ENSP00000370421.4:n.*26G>A
ENST00000381033.4:c.*26G>A ENSP00000370421.4:n.*26G>A
NM_000209.3:c.*26G>A NP_000200.1:n.*26G>A
NM_000209.4:c.*26G>A MANE Select NP_000200.1:n.*26G>A