Canonical Allele Identifier: CA387646766
Gene: PDX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.28498782A>T (hg19) chr13:g.27924645A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924645A>T , CM000675.2:g.27924645A>T GRCh38
NC_000013.10:g.28498782A>T , CM000675.1:g.28498782A>T GRCh37
NC_000013.9:g.27396782A>T NCBI36
NG_008183.1:g.9615A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.796A>T MANE Select ENSP00000370421.4:p.Ser266Cys
ENST00000381033.4:c.796A>T ENSP00000370421.4:p.Ser266Cys
NM_000209.3:c.796A>T NP_000200.1:p.Ser266Cys
NM_000209.4:c.796A>T MANE Select NP_000200.1:p.Ser266Cys
Search 100 bp 5'
Search 100 bp 3'