Canonical Allele Identifier: CA844969539

Gene: DPYS

Linked Data

• dbSNP Id: rs1172933243
• MyVariant Identifiers: chr8:g.105391572G>A (hg19) ; chr8:g.104379344G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.104379344G>A , CM000670.2:g.104379344G>A	GRCh38
NC_000008.10:g.105391572G>A , CM000670.1:g.105391572G>A	GRCh37
NC_000008.9:g.105460748G>A	NCBI36
NG_008840.1:g.92706C>T
NG_008840.2:g.92706C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521601.1:n.328+1840C>T