Canonical Allele Identifier: CA1807671303
Gene: DPYS HGNC NCBI

Linked Data

dbSNP Id: rs1564074089

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379244G>C , CM000670.2:g.104379244G>C GRCh38
NC_000008.10:g.105391472G>C , CM000670.1:g.105391472G>C GRCh37
NC_000008.9:g.105460648G>C NCBI36
NG_008840.1:g.92806C>G
NG_008840.2:g.92806C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000521601.1:n.328+1940C>G