Canonical Allele Identifier: CA6927677
Gene: PDX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1967589
ClinVar RCV Id: RCV002754961 RCV004067749
dbSNP Id: rs758448475
ExAC: 13:28498514 G / T
gnomAD v2: 13-28498514-G-T
gnomAD v3: 13-27924377-G-T
gnomAD v4: 13-27924377-G-T
MyVariant Identifiers: chr13:g.28498514G>T (hg19) chr13:g.27924377G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924377G>T , CM000675.2:g.27924377G>T GRCh38
NC_000013.10:g.28498514G>T , CM000675.1:g.28498514G>T GRCh37
NC_000013.9:g.27396514G>T NCBI36
NG_008183.1:g.9347G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.528G>T MANE Select ENSP00000370421.4:p.Arg176=
ENST00000381033.4:c.528G>T ENSP00000370421.4:p.Arg176=
NM_000209.3:c.528G>T NP_000200.1:p.Arg176=
NM_000209.4:c.528G>T MANE Select NP_000200.1:p.Arg176=
Search 100 bp 5'
Search 100 bp 3'