Canonical Allele Identifier: CA483175766
Gene: PDX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.28498529C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924392C>A , CM000675.2:g.27924392C>A GRCh38
NC_000013.10:g.28498529C>A , CM000675.1:g.28498529C>A GRCh37
NC_000013.9:g.27396529C>A NCBI36
NG_008183.1:g.9362C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.543C>A MANE Select ENSP00000370421.4:p.Val181=
ENST00000381033.4:c.543C>A ENSP00000370421.4:p.Val181=
NM_000209.3:c.543C>A NP_000200.1:p.Val181=
NM_000209.4:c.543C>A MANE Select NP_000200.1:p.Val181=
Search 100 bp 5'
Search 100 bp 3'