Canonical Allele Identifier: CA608987624
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1287678458
gnomAD v2: 13-28498382-G-A
MyVariant Identifiers: chr13:g.28498382G>A (hg19) chr13:g.27924245G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924245G>A , CM000675.2:g.27924245G>A GRCh38
NC_000013.10:g.28498382G>A , CM000675.1:g.28498382G>A GRCh37
NC_000013.9:g.27396382G>A NCBI36
NG_008183.1:g.9215G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.407-11G>A MANE Select ENSP00000370421.4:n.407-11G>A
ENST00000381033.4:c.407-11G>A ENSP00000370421.4:n.407-11G>A
NM_000209.3:c.407-11G>A NP_000200.1:n.407-11G>A
XR_941578.1:n.3534-11G>A
XR_941579.1:n.2133-11G>A
XR_941580.1:n.1049-11G>A
XR_941578.2:n.3546-11G>A
XR_941580.2:n.1061-11G>A
NM_000209.4:c.407-11G>A MANE Select NP_000200.1:n.407-11G>A
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