Canonical Allele Identifier: CA1807671267
Gene: DPYS HGNC NCBI

Linked Data

dbSNP Id: rs1588388546

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379170G>T , CM000670.2:g.104379170G>T GRCh38
NC_000008.10:g.105391398G>T , CM000670.1:g.105391398G>T GRCh37
NC_000008.9:g.105460574G>T NCBI36
NG_008840.1:g.92880C>A
NG_008840.2:g.92880C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000521601.1:n.328+2014C>A