Canonical Allele Identifier: CA483175521
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1247879678
MyVariant Identifiers: chr13:g.28498394C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924257C>G , CM000675.2:g.27924257C>G GRCh38
NC_000013.10:g.28498394C>G , CM000675.1:g.28498394C>G GRCh37
NC_000013.9:g.27396394C>G NCBI36
NG_008183.1:g.9227C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.408C>G MANE Select ENSP00000370421.4:p.Gly136=
ENST00000381033.4:c.408C>G ENSP00000370421.4:p.Gly136=
NM_000209.3:c.408C>G NP_000200.1:p.Gly136=
XR_941578.1:n.3535C>G
XR_941579.1:n.2134C>G
XR_941580.1:n.1050C>G
XR_941578.2:n.3547C>G
XR_941580.2:n.1062C>G
NM_000209.4:c.408C>G MANE Select NP_000200.1:p.Gly136=