Canonical Allele Identifier: CA247265681
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs950269577
gnomAD v2: 13-28498841-G-A
gnomAD v3: 13-27924704-G-A
gnomAD v4: 13-27924704-G-A
MyVariant Identifiers: chr13:g.28498841G>A (hg19) chr13:g.27924704G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924704G>A , CM000675.2:g.27924704G>A GRCh38
NC_000013.10:g.28498841G>A , CM000675.1:g.28498841G>A GRCh37
NC_000013.9:g.27396841G>A NCBI36
NG_008183.1:g.9674G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*3G>A MANE Select ENSP00000370421.4:n.*3G>A
ENST00000381033.4:c.*3G>A ENSP00000370421.4:n.*3G>A
NM_000209.3:c.*3G>A NP_000200.1:n.*3G>A
NM_000209.4:c.*3G>A MANE Select NP_000200.1:n.*3G>A
Search 100 bp 5'
Search 100 bp 3'