Canonical Allele Identifier: CA697009632
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1222929444
gnomAD v3: 13-27924801-T-G
gnomAD v4: 13-27924801-T-G
MyVariant Identifiers: chr13:g.28498938T>G (hg19) chr13:g.27924801T>G (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

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