Canonical Allele Identifier: CA1807671311
Gene: DPYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379265T= , CM000670.2:g.104379265T= GRCh38
NC_000008.10:g.105391493T= , CM000670.1:g.105391493T= GRCh37
NC_000008.9:g.105460669T= NCBI36
NG_008840.1:g.92785A=
NG_008840.2:g.92785A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000521601.1:n.328+1919A=