Canonical Allele Identifier: CA2718084433
Gene: DPYS HGNC NCBI

Linked Data

dbSNP Id: rs2140492489

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379204C>T , CM000670.2:g.104379204C>T GRCh38
NC_000008.10:g.105391432C>T , CM000670.1:g.105391432C>T GRCh37
NC_000008.9:g.105460608C>T NCBI36
NG_008840.1:g.92846G>A
NG_008840.2:g.92846G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000521601.1:n.328+1980G>A