Canonical Allele Identifier: CA1807671286
Gene: DPYS HGNC NCBI

Linked Data

dbSNP Id: rs1810949974

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379203C>T , CM000670.2:g.104379203C>T GRCh38
NC_000008.10:g.105391431C>T , CM000670.1:g.105391431C>T GRCh37
NC_000008.9:g.105460607C>T NCBI36
NG_008840.1:g.92847G>A
NG_008840.2:g.92847G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000521601.1:n.328+1981G>A