Canonical Allele Identifier: CA182608759

Gene: DPYS

Linked Data

• dbSNP Id: rs754894369
• MyVariant Identifiers: chr8:g.105391529T>C (hg19) ; chr8:g.104379301T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.104379301T>C , CM000670.2:g.104379301T>C	GRCh38
NC_000008.10:g.105391529T>C , CM000670.1:g.105391529T>C	GRCh37
NC_000008.9:g.105460705T>C	NCBI36
NG_008840.1:g.92749A>G
NG_008840.2:g.92749A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521601.1:n.328+1883A>G