Canonical Allele Identifier: CA718913144

Gene: UMOD

Linked Data

• dbSNP Id: rs1225562496
• MyVariant Identifiers: chr16:g.20364499C>T (hg19) ; chr16:g.20353177C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.20353177C>T , CM000678.2:g.20353177C>T	GRCh38
NC_000016.9:g.20364499C>T , CM000678.1:g.20364499C>T	GRCh37
NC_000016.8:g.20272000C>T	NCBI36
NG_008151.1:g.4539G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000570689.5:c.-39-2401G>A	ENSP00000460548.1:n.-39-2401G>A
XM_011545938.1:c.-39-2401G>A	XP_011544240.1:n.-39-2401G>A