Canonical Allele Identifier: CA2556881919
Gene: DPYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379149A>T , CM000670.2:g.104379149A>T GRCh38
NC_000008.10:g.105391377A>T , CM000670.1:g.105391377A>T GRCh37
NC_000008.9:g.105460553A>T NCBI36
NG_008840.1:g.92901T>A
NG_008840.2:g.92901T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000521601.1:n.328+2035T>A