Canonical Allele Identifier: CA718913118

Gene: UMOD

Linked Data

• dbSNP Id: rs1296173201
• gnomAD v3: 16-20353082-G-A
• gnomAD v4: 16-20353082-G-A
• MyVariant Identifiers: chr16:g.20364404G>A (hg19) ; chr16:g.20353082G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.20353082G>A , CM000678.2:g.20353082G>A	GRCh38
NC_000016.9:g.20364404G>A , CM000678.1:g.20364404G>A	GRCh37
NC_000016.8:g.20271905G>A	NCBI36
NG_008151.1:g.4634C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570689.5:c.-39-2306C>T	ENSP00000460548.1:n.-39-2306C>T
XM_011545938.1:c.-39-2306C>T	XP_011544240.1:n.-39-2306C>T