Canonical Allele Identifier: CA1807671264
Gene: DPYS HGNC NCBI

Linked Data

dbSNP Id: rs1810948842

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379169G>T , CM000670.2:g.104379169G>T GRCh38
NC_000008.10:g.105391397G>T , CM000670.1:g.105391397G>T GRCh37
NC_000008.9:g.105460573G>T NCBI36
NG_008840.1:g.92881C>A
NG_008840.2:g.92881C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000521601.1:n.328+2015C>A