Canonical Allele Identifier: CA697009633
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1374183054

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924804A>C , CM000675.2:g.27924804A>C GRCh38
NC_000013.10:g.28498941A>C , CM000675.1:g.28498941A>C GRCh37
NC_000013.9:g.27396941A>C NCBI36
NG_008183.1:g.9774A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*103A>C MANE Select ENSP00000370421.4:n.*103A>C
ENST00000381033.4:c.*103A>C ENSP00000370421.4:n.*103A>C
NM_000209.3:c.*103A>C NP_000200.1:n.*103A>C
NM_000209.4:c.*103A>C MANE Select NP_000200.1:n.*103A>C