Canonical Allele Identifier: CA483026947
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1375644348
gnomAD v2: 13-28498736-C-T
gnomAD v4: 13-27924599-C-T
MyVariant Identifiers: chr13:g.28498736C>T (hg19) chr13:g.27924599C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924599C>T , CM000675.2:g.27924599C>T GRCh38
NC_000013.10:g.28498736C>T , CM000675.1:g.28498736C>T GRCh37
NC_000013.9:g.27396736C>T NCBI36
NG_008183.1:g.9569C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.750C>T MANE Select ENSP00000370421.4:p.Pro250=
ENST00000381033.4:c.750C>T ENSP00000370421.4:p.Pro250=
NM_000209.3:c.750C>T NP_000200.1:p.Pro250=
NM_000209.4:c.750C>T MANE Select NP_000200.1:p.Pro250=
Search 100 bp 5'
Search 100 bp 3'