Canonical Allele Identifier: CA12735227
Gene: DPYS HGNC NCBI

Linked Data

dbSNP Id: rs4734782

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104362428C>A , CM000670.2:g.104362428C>A GRCh38
NC_000008.10:g.105374656C>A , CM000670.1:g.105374656C>A GRCh37
NC_000008.9:g.105443832C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000521601.1:n.328+18756G>T