Canonical Allele Identifier: CA1807671249
Gene: DPYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379142A= , CM000670.2:g.104379142A= GRCh38
NC_000008.10:g.105391370A= , CM000670.1:g.105391370A= GRCh37
NC_000008.9:g.105460546A= NCBI36
NG_008840.1:g.92908T=
NG_008840.2:g.92908T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000521601.1:n.328+2042T=