Canonical Allele Identifier: CA27624661
Gene: DPYD HGNC NCBI

Linked Data

dbSNP Id: rs1033092437
MyVariant Identifiers: chr1:g.97691712T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97691712T>C , CM000663.2:g.97691712T>C GRCh38
NC_000001.10:g.98157268T>C , CM000663.1:g.98157268T>C GRCh37
NC_000001.9:g.97929856T>C NCBI36
NG_008807.2:g.234348A>G , LRG_722:g.234348A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.762+5A>G MANE Select ENSP00000359211.3:n.762+5A>G
ENST00000370192.7:c.762+5A>G ENSP00000359211.3:n.762+5A>G
ENST00000474241.1:n.531A>G
NM_000110.3:c.762+5A>G , LRG_722t1:c.762+5A>G NP_000101.2:n.762+5A>G
XM_005270562.3:c.762+5A>G XP_005270619.2:n.762+5A>G
XM_006710397.2:c.762+5A>G XP_006710460.1:n.762+5A>G
XM_006710397.3:c.762+5A>G XP_006710460.1:n.762+5A>G
XM_017000507.1:c.651+5A>G XP_016855996.1:n.651+5A>G
XM_017000508.2:c.267+5A>G XP_016855997.1:n.267+5A>G
XM_017000509.2:c.267+5A>G XP_016855998.1:n.267+5A>G
XM_017000510.1:c.267+5A>G XP_016855999.1:n.267+5A>G
NM_000110.4:c.762+5A>G MANE Select NP_000101.2:n.762+5A>G