Canonical Allele Identifier: CA718913143

Gene: UMOD

Linked Data

• dbSNP Id: rs1263880736
• gnomAD v3: 16-20353176-A-G
• gnomAD v4: 16-20353176-A-G
• MyVariant Identifiers: chr16:g.20364498A>G (hg19) ; chr16:g.20353176A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.20353176A>G , CM000678.2:g.20353176A>G	GRCh38
NC_000016.9:g.20364498A>G , CM000678.1:g.20364498A>G	GRCh37
NC_000016.8:g.20271999A>G	NCBI36
NG_008151.1:g.4540T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000570689.5:c.-39-2400T>C	ENSP00000460548.1:n.-39-2400T>C
XM_011545938.1:c.-39-2400T>C	XP_011544240.1:n.-39-2400T>C