Canonical Allele Identifier: CA483176114
Gene: PDX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.28498673G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924536G>A , CM000675.2:g.27924536G>A GRCh38
NC_000013.10:g.28498673G>A , CM000675.1:g.28498673G>A GRCh37
NC_000013.9:g.27396673G>A NCBI36
NG_008183.1:g.9506G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.687G>A MANE Select ENSP00000370421.4:p.Val229=
ENST00000381033.4:c.687G>A ENSP00000370421.4:p.Val229=
NM_000209.3:c.687G>A NP_000200.1:p.Val229=
NM_000209.4:c.687G>A MANE Select NP_000200.1:p.Val229=
Search 100 bp 5'
Search 100 bp 3'