Canonical Allele Identifier: CA279253558

Gene: UMOD

Linked Data

• dbSNP Id: rs767520765
• gnomAD v3: 16-20353285-C-G
• gnomAD v4: 16-20353285-C-G
• MyVariant Identifiers: chr16:g.20364607C>G (hg19) ; chr16:g.20353285C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.20353285C>G , CM000678.2:g.20353285C>G	GRCh38
NC_000016.9:g.20364607C>G , CM000678.1:g.20364607C>G	GRCh37
NC_000016.8:g.20272108C>G	NCBI36
NG_008151.1:g.4431G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000570689.5:c.-39-2509G>C	ENSP00000460548.1:n.-39-2509G>C
XM_011545938.1:c.-39-2509G>C	XP_011544240.1:n.-39-2509G>C