Canonical Allele Identifier: CA844969447
Gene: DPYS HGNC NCBI

Linked Data

dbSNP Id: rs1218777275
MyVariant Identifiers: chr8:g.105391366T>A (hg19) chr8:g.104379138T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379138T>A , CM000670.2:g.104379138T>A GRCh38
NC_000008.10:g.105391366T>A , CM000670.1:g.105391366T>A GRCh37
NC_000008.9:g.105460542T>A NCBI36
NG_008840.1:g.92912A>T
NG_008840.2:g.92912A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000521601.1:n.328+2046A>T
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