Canonical Allele Identifier: CA697009623
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1234487424
gnomAD v4: 13-27924763-T-C
MyVariant Identifiers: chr13:g.28498900T>C (hg19) chr13:g.27924763T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924763T>C , CM000675.2:g.27924763T>C GRCh38
NC_000013.10:g.28498900T>C , CM000675.1:g.28498900T>C GRCh37
NC_000013.9:g.27396900T>C NCBI36
NG_008183.1:g.9733T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*62T>C MANE Select ENSP00000370421.4:n.*62T>C
ENST00000381033.4:c.*62T>C ENSP00000370421.4:n.*62T>C
NM_000209.3:c.*62T>C NP_000200.1:n.*62T>C
NM_000209.4:c.*62T>C MANE Select NP_000200.1:n.*62T>C
Search 100 bp 5'
Search 100 bp 3'