Canonical Allele Identifier: CA718913217

Gene: UMOD

Linked Data

• dbSNP Id: rs1382017828
• gnomAD v3: 16-20353353-C-T
• gnomAD v4: 16-20353353-C-T
• MyVariant Identifiers: chr16:g.20364675C>T (hg19) ; chr16:g.20353353C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.20353353C>T , CM000678.2:g.20353353C>T	GRCh38
NC_000016.9:g.20364675C>T , CM000678.1:g.20364675C>T	GRCh37
NC_000016.8:g.20272176C>T	NCBI36
NG_008151.1:g.4363G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570689.5:c.-39-2577G>A	ENSP00000460548.1:n.-39-2577G>A
XM_011545938.1:c.-39-2577G>A	XP_011544240.1:n.-39-2577G>A