Canonical Allele Identifier: CA844969462
Gene: DPYS HGNC NCBI

Linked Data

dbSNP Id: rs1398857899
MyVariant Identifiers: chr8:g.105391387G>T (hg19) chr8:g.104379159G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379159G>T , CM000670.2:g.104379159G>T GRCh38
NC_000008.10:g.105391387G>T , CM000670.1:g.105391387G>T GRCh37
NC_000008.9:g.105460563G>T NCBI36
NG_008840.1:g.92891C>A
NG_008840.2:g.92891C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000521601.1:n.328+2025C>A
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