Canonical Allele Identifier: CA1807671277
Gene: DPYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379184T= , CM000670.2:g.104379184T= GRCh38
NC_000008.10:g.105391412T= , CM000670.1:g.105391412T= GRCh37
NC_000008.9:g.105460588T= NCBI36
NG_008840.1:g.92866A=
NG_008840.2:g.92866A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000521601.1:n.328+2000A=