Canonical Allele Identifier: CA608987625
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1450909620
gnomAD v2: 13-28498383-T-C
gnomAD v4: 13-27924246-T-C
MyVariant Identifiers: chr13:g.28498383T>C (hg19) chr13:g.27924246T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924246T>C , CM000675.2:g.27924246T>C GRCh38
NC_000013.10:g.28498383T>C , CM000675.1:g.28498383T>C GRCh37
NC_000013.9:g.27396383T>C NCBI36
NG_008183.1:g.9216T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.407-10T>C MANE Select ENSP00000370421.4:n.407-10T>C
ENST00000381033.4:c.407-10T>C ENSP00000370421.4:n.407-10T>C
NM_000209.3:c.407-10T>C NP_000200.1:n.407-10T>C
XR_941578.1:n.3534-10T>C
XR_941579.1:n.2133-10T>C
XR_941580.1:n.1049-10T>C
XR_941578.2:n.3546-10T>C
XR_941580.2:n.1061-10T>C
NM_000209.4:c.407-10T>C MANE Select NP_000200.1:n.407-10T>C
Search 100 bp 5'
Search 100 bp 3'