Canonical Allele Identifier: CA27624667

Gene: DPYD

Linked Data

• dbSNP Id: rs6675198
• gnomAD v4: 1-97691723-A-G
• MyVariant Identifiers: chr1:g.98157279A>G (hg19) ; chr1:g.97691723A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691723A>G , CM000663.2:g.97691723A>G	GRCh38
NC_000001.10:g.98157279A>G , CM000663.1:g.98157279A>G	GRCh37
NC_000001.9:g.97929867A>G	NCBI36
NG_008807.2:g.234337T>C , LRG_722:g.234337T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.756T>C MANE Select	ENSP00000359211.3:p.Gly252=
ENST00000370192.7:c.756T>C	ENSP00000359211.3:p.Gly252=
ENST00000474241.1:n.520T>C
NM_000110.3:c.756T>C , LRG_722t1:c.756T>C	NP_000101.2:p.Gly252=
XM_005270562.3:c.756T>C	XP_005270619.2:p.Gly252=
XM_006710397.2:c.756T>C	XP_006710460.1:p.Gly252=
XM_006710397.3:c.756T>C	XP_006710460.1:p.Gly252=
XM_017000507.1:c.645T>C	XP_016855996.1:p.Gly215=
XM_017000508.2:c.261T>C	XP_016855997.1:p.Gly87=
XM_017000509.2:c.261T>C	XP_016855998.1:p.Gly87=
XM_017000510.1:c.261T>C	XP_016855999.1:p.Gly87=
NM_000110.4:c.756T>C MANE Select	NP_000101.2:p.Gly252=