Canonical Allele Identifier: CA483175692
Gene: PDX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.28498490C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924353C>T , CM000675.2:g.27924353C>T GRCh38
NC_000013.10:g.28498490C>T , CM000675.1:g.28498490C>T GRCh37
NC_000013.9:g.27396490C>T NCBI36
NG_008183.1:g.9323C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.504C>T MANE Select ENSP00000370421.4:p.Asn168=
ENST00000381033.4:c.504C>T ENSP00000370421.4:p.Asn168=
NM_000209.3:c.504C>T NP_000200.1:p.Asn168=
NM_000209.4:c.504C>T MANE Select NP_000200.1:p.Asn168=
Search 100 bp 5'
Search 100 bp 3'