Canonical Allele Identifier: CA483175973
Gene: PDX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.28498616C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924479C>G , CM000675.2:g.27924479C>G GRCh38
NC_000013.10:g.28498616C>G , CM000675.1:g.28498616C>G GRCh37
NC_000013.9:g.27396616C>G NCBI36
NG_008183.1:g.9449C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.630C>G MANE Select ENSP00000370421.4:p.Gly210=
ENST00000381033.4:c.630C>G ENSP00000370421.4:p.Gly210=
NM_000209.3:c.630C>G NP_000200.1:p.Gly210=
NM_000209.4:c.630C>G MANE Select NP_000200.1:p.Gly210=
Search 100 bp 5'
Search 100 bp 3'