Canonical Allele Identifier: CA16344424
Gene: DPYS HGNC NCBI

Linked Data

dbSNP Id: rs59980026
gnomAD v2: 8-105391381-A-C
gnomAD v3: 8-104379153-A-C
gnomAD v4: 8-104379153-A-C
MyVariant Identifiers: chr8:g.105391381A>C (hg19) chr8:g.104379153A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379153A>C , CM000670.2:g.104379153A>C GRCh38
NC_000008.10:g.105391381A>C , CM000670.1:g.105391381A>C GRCh37
NC_000008.9:g.105460557A>C NCBI36
NG_008840.1:g.92897T>G
NG_008840.2:g.92897T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000521601.1:n.328+2031T>G
Search 100 bp 5'
Search 100 bp 3'