Canonical Allele Identifier: CA387646985
Gene: PDX1 HGNC NCBI

Linked Data

gnomAD v4: 13-27924699-T-C
MyVariant Identifiers: chr13:g.28498836T>C (hg19) chr13:g.27924699T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924699T>C , CM000675.2:g.27924699T>C GRCh38
NC_000013.10:g.28498836T>C , CM000675.1:g.28498836T>C GRCh37
NC_000013.9:g.27396836T>C NCBI36
NG_008183.1:g.9669T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.850T>C MANE Select ENSP00000370421.4:p.Ter284Arg
ENST00000381033.4:c.850T>C ENSP00000370421.4:p.Ter284Arg
NM_000209.3:c.850T>C NP_000200.1:p.Ter284Arg
NM_000209.4:c.850T>C MANE Select NP_000200.1:p.Ter284Arg
Search 100 bp 5'
Search 100 bp 3'