Canonical Allele Identifier: CA1807671386
Gene: DPYS HGNC NCBI

Linked Data

dbSNP Id: rs1588388725

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379426A>C , CM000670.2:g.104379426A>C GRCh38
NC_000008.10:g.105391654A>C , CM000670.1:g.105391654A>C GRCh37
NC_000008.9:g.105460830A>C NCBI36
NG_008840.1:g.92624T>G
NG_008840.2:g.92624T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000351513.6:c.*432T>G ENSP00000276651.2:n.*432T>G
ENST00000521601.1:n.328+1758T>G
NM_001385.2:c.*432T>G NP_001376.1:n.*432T>G