Canonical Allele Identifier: CA483175957
Gene: PDX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.28498610G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924473G>A , CM000675.2:g.27924473G>A GRCh38
NC_000013.10:g.28498610G>A , CM000675.1:g.28498610G>A GRCh37
NC_000013.9:g.27396610G>A NCBI36
NG_008183.1:g.9443G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.624G>A MANE Select ENSP00000370421.4:p.Lys208=
ENST00000381033.4:c.624G>A ENSP00000370421.4:p.Lys208=
NM_000209.3:c.624G>A NP_000200.1:p.Lys208=
NM_000209.4:c.624G>A MANE Select NP_000200.1:p.Lys208=
Search 100 bp 5'
Search 100 bp 3'