Canonical Allele Identifier: CA844969472
Gene: DPYS HGNC NCBI

Linked Data

dbSNP Id: rs1299485714
MyVariant Identifiers: chr8:g.105391394G>C (hg19) chr8:g.104379166G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379166G>C , CM000670.2:g.104379166G>C GRCh38
NC_000008.10:g.105391394G>C , CM000670.1:g.105391394G>C GRCh37
NC_000008.9:g.105460570G>C NCBI36
NG_008840.1:g.92884C>G
NG_008840.2:g.92884C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000521601.1:n.328+2018C>G
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