Canonical Allele Identifier: CA2080721180
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1566025444

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924233C>G , CM000675.2:g.27924233C>G GRCh38
NC_000013.10:g.28498370C>G , CM000675.1:g.28498370C>G GRCh37
NC_000013.9:g.27396370C>G NCBI36
NG_008183.1:g.9203C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.407-23C>G MANE Select ENSP00000370421.4:n.407-23C>G
ENST00000381033.4:c.407-23C>G ENSP00000370421.4:n.407-23C>G
NM_000209.3:c.407-23C>G NP_000200.1:n.407-23C>G
XR_941578.1:n.3534-23C>G
XR_941579.1:n.2133-23C>G
XR_941580.1:n.1049-23C>G
XR_941578.2:n.3546-23C>G
XR_941580.2:n.1061-23C>G
NM_000209.4:c.407-23C>G MANE Select NP_000200.1:n.407-23C>G