Canonical Allele Identifier: CA1807671355
Gene: DPYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379363A= , CM000670.2:g.104379363A= GRCh38
NC_000008.10:g.105391591A= , CM000670.1:g.105391591A= GRCh37
NC_000008.9:g.105460767A= NCBI36
NG_008840.1:g.92687T=
NG_008840.2:g.92687T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000521601.1:n.328+1821T=