Canonical Allele Identifier: CA1807671248
Gene: DPYS HGNC NCBI

Linked Data

dbSNP Id: rs1588388496
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379139A>C , CM000670.2:g.104379139A>C GRCh38
NC_000008.10:g.105391367A>C , CM000670.1:g.105391367A>C GRCh37
NC_000008.9:g.105460543A>C NCBI36
NG_008840.1:g.92911T>G
NG_008840.2:g.92911T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000521601.1:n.328+2045T>G
Search 100 bp 5'
Search 100 bp 3'