Canonical Allele Identifier: CA1807671310
Gene: DPYS HGNC NCBI

Linked Data

dbSNP Id: rs1810951505

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379267del , CM000670.2:g.104379267del GRCh38
NC_000008.10:g.105391495del , CM000670.1:g.105391495del GRCh37
NC_000008.9:g.105460671del NCBI36
NG_008840.1:g.92786del
NG_008840.2:g.92786del

Transcript Alleles

HGVS Amino-acid Change
ENST00000521601.1:n.328+1920del