Canonical Allele Identifier: CA387645498
Gene: PDX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.28498496C>A (hg19) chr13:g.27924359C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924359C>A , CM000675.2:g.27924359C>A GRCh38
NC_000013.10:g.28498496C>A , CM000675.1:g.28498496C>A GRCh37
NC_000013.9:g.27396496C>A NCBI36
NG_008183.1:g.9329C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.510C>A MANE Select ENSP00000370421.4:p.Tyr170Ter
ENST00000381033.4:c.510C>A ENSP00000370421.4:p.Tyr170Ter
NM_000209.3:c.510C>A NP_000200.1:p.Tyr170Ter
NM_000209.4:c.510C>A MANE Select NP_000200.1:p.Tyr170Ter
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