Canonical Allele Identifier: CA387645370
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1456103730
gnomAD v2: 13-28498450-G-T
gnomAD v4: 13-27924313-G-T
MyVariant Identifiers: chr13:g.28498450G>T (hg19) chr13:g.27924313G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924313G>T , CM000675.2:g.27924313G>T GRCh38
NC_000013.10:g.28498450G>T , CM000675.1:g.28498450G>T GRCh37
NC_000013.9:g.27396450G>T NCBI36
NG_008183.1:g.9283G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.464G>T MANE Select ENSP00000370421.4:p.Arg155Leu
ENST00000381033.4:c.464G>T ENSP00000370421.4:p.Arg155Leu
NM_000209.3:c.464G>T NP_000200.1:p.Arg155Leu
XR_941579.1:n.2190G>T
XR_941580.1:n.1106G>T
XR_941580.2:n.1118G>T
NM_000209.4:c.464G>T MANE Select NP_000200.1:p.Arg155Leu
Search 100 bp 5'
Search 100 bp 3'