Canonical Allele Identifier: CA6927658
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs549332437
ExAC: 13:28498385 G / T
gnomAD v2: 13-28498385-G-T
gnomAD v3: 13-27924248-G-T
gnomAD v4: 13-27924248-G-T
MyVariant Identifiers: chr13:g.28498385G>T (hg19) chr13:g.27924248G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924248G>T , CM000675.2:g.27924248G>T GRCh38
NC_000013.10:g.28498385G>T , CM000675.1:g.28498385G>T GRCh37
NC_000013.9:g.27396385G>T NCBI36
NG_008183.1:g.9218G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.407-8G>T MANE Select ENSP00000370421.4:n.407-8G>T
ENST00000381033.4:c.407-8G>T ENSP00000370421.4:n.407-8G>T
NM_000209.3:c.407-8G>T NP_000200.1:n.407-8G>T
XR_941578.1:n.3534-8G>T
XR_941579.1:n.2133-8G>T
XR_941580.1:n.1049-8G>T
XR_941578.2:n.3546-8G>T
XR_941580.2:n.1061-8G>T
NM_000209.4:c.407-8G>T MANE Select NP_000200.1:n.407-8G>T
Search 100 bp 5'
Search 100 bp 3'