Canonical Allele Identifier: CA247265682
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs907660995

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924706C>T , CM000675.2:g.27924706C>T GRCh38
NC_000013.10:g.28498843C>T , CM000675.1:g.28498843C>T GRCh37
NC_000013.9:g.27396843C>T NCBI36
NG_008183.1:g.9676C>T

Transcript Alleles

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