Canonical Allele Identifier: CA1807671379
Gene: DPYS HGNC NCBI

Linked Data

dbSNP Id: rs1810957561
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379412T>A , CM000670.2:g.104379412T>A GRCh38
NC_000008.10:g.105391640T>A , CM000670.1:g.105391640T>A GRCh37
NC_000008.9:g.105460816T>A NCBI36
NG_008840.1:g.92638A>T
NG_008840.2:g.92638A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000521601.1:n.328+1772A>T
Search 100 bp 5'
Search 100 bp 3'