Canonical Allele Identifier: CA387645352
Gene: PDX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.28498441C>G (hg19) chr13:g.27924304C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924304C>G , CM000675.2:g.27924304C>G GRCh38
NC_000013.10:g.28498441C>G , CM000675.1:g.28498441C>G GRCh37
NC_000013.9:g.27396441C>G NCBI36
NG_008183.1:g.9274C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.455C>G MANE Select ENSP00000370421.4:p.Ala152Gly
ENST00000381033.4:c.455C>G ENSP00000370421.4:p.Ala152Gly
NM_000209.3:c.455C>G NP_000200.1:p.Ala152Gly
XR_941579.1:n.2181C>G
XR_941580.1:n.1097C>G
XR_941578.2:n.3594C>G
XR_941580.2:n.1109C>G
NM_000209.4:c.455C>G MANE Select NP_000200.1:p.Ala152Gly
Search 100 bp 5'
Search 100 bp 3'