Canonical Allele Identifier: CA621251026

Gene: UMOD

Linked Data

• dbSNP Id: rs1420979263
• gnomAD v2: 16-20364617-C-A
• gnomAD v3: 16-20353295-C-A
• gnomAD v4: 16-20353295-C-A
• MyVariant Identifiers: chr16:g.20364617C>A (hg19) ; chr16:g.20353295C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.20353295C>A , CM000678.2:g.20353295C>A	GRCh38
NC_000016.9:g.20364617C>A , CM000678.1:g.20364617C>A	GRCh37
NC_000016.8:g.20272118C>A	NCBI36
NG_008151.1:g.4421G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000570689.5:c.-39-2519G>T	ENSP00000460548.1:n.-39-2519G>T
XM_011545938.1:c.-39-2519G>T	XP_011544240.1:n.-39-2519G>T