Canonical Allele Identifier: CA1117446079
Gene: DPYS HGNC NCBI

Linked Data

dbSNP Id: rs1810951250

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379256T>C , CM000670.2:g.104379256T>C GRCh38
NC_000008.10:g.105391484T>C , CM000670.1:g.105391484T>C GRCh37
NC_000008.9:g.105460660T>C NCBI36
NG_008840.1:g.92794A>G
NG_008840.2:g.92794A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000521601.1:n.328+1928A>G