Canonical Allele Identifier: CA1807671326
Gene: DPYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379298T= , CM000670.2:g.104379298T= GRCh38
NC_000008.10:g.105391526T= , CM000670.1:g.105391526T= GRCh37
NC_000008.9:g.105460702T= NCBI36
NG_008840.1:g.92752A=
NG_008840.2:g.92752A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000521601.1:n.328+1886A=