Canonical Allele Identifier: CA387645954
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1957810066

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924442G>C , CM000675.2:g.27924442G>C GRCh38
NC_000013.10:g.28498579G>C , CM000675.1:g.28498579G>C GRCh37
NC_000013.9:g.27396579G>C NCBI36
NG_008183.1:g.9412G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.593G>C MANE Select ENSP00000370421.4:p.Arg198Pro
ENST00000381033.4:c.593G>C ENSP00000370421.4:p.Arg198Pro
NM_000209.3:c.593G>C NP_000200.1:p.Arg198Pro
NM_000209.4:c.593G>C MANE Select NP_000200.1:p.Arg198Pro