Canonical Allele Identifier: CA6927689
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs776932903
ExAC: 13:28498619 C / T
gnomAD v2: 13-28498619-C-T
gnomAD v4: 13-27924482-C-T
MyVariant Identifiers: chr13:g.28498619C>T (hg19) chr13:g.27924482C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924482C>T , CM000675.2:g.27924482C>T GRCh38
NC_000013.10:g.28498619C>T , CM000675.1:g.28498619C>T GRCh37
NC_000013.9:g.27396619C>T NCBI36
NG_008183.1:g.9452C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.633C>T MANE Select ENSP00000370421.4:p.Gly211=
ENST00000381033.4:c.633C>T ENSP00000370421.4:p.Gly211=
NM_000209.3:c.633C>T NP_000200.1:p.Gly211=
NM_000209.4:c.633C>T MANE Select NP_000200.1:p.Gly211=
Search 100 bp 5'
Search 100 bp 3'