Canonical Allele Identifier: CA387645429
Gene: PDX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.28498477A>G (hg19) chr13:g.27924340A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924340A>G , CM000675.2:g.27924340A>G GRCh38
NC_000013.10:g.28498477A>G , CM000675.1:g.28498477A>G GRCh37
NC_000013.9:g.27396477A>G NCBI36
NG_008183.1:g.9310A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.491A>G MANE Select ENSP00000370421.4:p.Glu164Gly
ENST00000381033.4:c.491A>G ENSP00000370421.4:p.Glu164Gly
NM_000209.3:c.491A>G NP_000200.1:p.Glu164Gly
NM_000209.4:c.491A>G MANE Select NP_000200.1:p.Glu164Gly
Search 100 bp 5'
Search 100 bp 3'