Canonical Allele Identifier: CA6927662
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs775275110
ExAC: 13:28498406 T / C
gnomAD v2: 13-28498406-T-C
gnomAD v4: 13-27924269-T-C
MyVariant Identifiers: chr13:g.28498406T>C (hg19) chr13:g.27924269T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924269T>C , CM000675.2:g.27924269T>C GRCh38
NC_000013.10:g.28498406T>C , CM000675.1:g.28498406T>C GRCh37
NC_000013.9:g.27396406T>C NCBI36
NG_008183.1:g.9239T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.420T>C MANE Select ENSP00000370421.4:p.Ala140=
ENST00000381033.4:c.420T>C ENSP00000370421.4:p.Ala140=
NM_000209.3:c.420T>C NP_000200.1:p.Ala140=
XR_941578.1:n.3547T>C
XR_941579.1:n.2146T>C
XR_941580.1:n.1062T>C
XR_941578.2:n.3559T>C
XR_941580.2:n.1074T>C
NM_000209.4:c.420T>C MANE Select NP_000200.1:p.Ala140=
Search 100 bp 5'
Search 100 bp 3'