Canonical Allele Identifier: CA2622478539
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924778C>T , CM000675.2:g.27924778C>T GRCh38
NC_000013.10:g.28498915C>T , CM000675.1:g.28498915C>T GRCh37
NC_000013.9:g.27396915C>T NCBI36
NG_008183.1:g.9748C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*77C>T MANE Select ENSP00000370421.4:n.*77C>T
ENST00000381033.4:c.*77C>T ENSP00000370421.4:n.*77C>T
NM_000209.3:c.*77C>T NP_000200.1:n.*77C>T
NM_000209.4:c.*77C>T MANE Select NP_000200.1:n.*77C>T