Canonical Allele Identifier: CA1807671308
Gene: DPYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379260C= , CM000670.2:g.104379260C= GRCh38
NC_000008.10:g.105391488C= , CM000670.1:g.105391488C= GRCh37
NC_000008.9:g.105460664C= NCBI36
NG_008840.1:g.92790G=
NG_008840.2:g.92790G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000521601.1:n.328+1924G=