Canonical Allele Identifier: CA844969476
Gene: DPYS HGNC NCBI

Linked Data

dbSNP Id: rs1323349106
MyVariant Identifiers: chr8:g.105391397del (hg19) chr8:g.104379169del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379170del , CM000670.2:g.104379170del GRCh38
NC_000008.10:g.105391398del , CM000670.1:g.105391398del GRCh37
NC_000008.9:g.105460574del NCBI36
NG_008840.1:g.92881del
NG_008840.2:g.92881del

Transcript Alleles

HGVS Amino-acid Change
ENST00000521601.1:n.328+2015del
Search 100 bp 5'
Search 100 bp 3'