Canonical Allele Identifier: CA2718084391
Gene: DPYS HGNC NCBI

Linked Data

dbSNP Id: rs2140492481

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379200A>T , CM000670.2:g.104379200A>T GRCh38
NC_000008.10:g.105391428A>T , CM000670.1:g.105391428A>T GRCh37
NC_000008.9:g.105460604A>T NCBI36
NG_008840.1:g.92850T>A
NG_008840.2:g.92850T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000521601.1:n.328+1984T>A