Canonical Allele Identifier: CA954374547
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1222929444
gnomAD v3: 13-27924801-T-C
gnomAD v4: 13-27924801-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924801T>C , CM000675.2:g.27924801T>C GRCh38
NC_000013.10:g.28498938T>C , CM000675.1:g.28498938T>C GRCh37
NC_000013.9:g.27396938T>C NCBI36
NG_008183.1:g.9771T>C

Transcript Alleles

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