Canonical Allele Identifier: CA6927705
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs746545394

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924524G>A , CM000675.2:g.27924524G>A GRCh38
NC_000013.10:g.28498661G>A , CM000675.1:g.28498661G>A GRCh37
NC_000013.9:g.27396661G>A NCBI36
NG_008183.1:g.9494G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.675G>A MANE Select ENSP00000370421.4:p.Gln225=
ENST00000381033.4:c.675G>A ENSP00000370421.4:p.Gln225=
NM_000209.3:c.675G>A NP_000200.1:p.Gln225=
NM_000209.4:c.675G>A MANE Select NP_000200.1:p.Gln225=